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5962-0151801QYC 参数 Datasheet PDF下载

5962-0151801QYC图片预览
型号: 5962-0151801QYC
PDF下载: 下载PDF文件 查看货源
内容描述: [Field Programmable Gate Array, 32000 Gates, 206MHz, 2880-Cell, CMOS, CQFP208, CERAMIC, QFP-208]
分类和应用: 可编程逻辑
文件页数/大小: 217 页 / 1554 K
品牌: ACTEL [ Actel Corporation ]
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MIL-PRF-38535K  
APPENDIX A  
(2) Control procedures for lot history records:  
(a) Lot histories may be modified only by additions (e.g., original entries plus corrective addenda).  
(b) All corrective addenda shall meet all the requirements of A.4.8.1.2 i.  
(c) Only limited designated operators shall be able to access lot history computer records for corrective  
addenda. Documented security procedures shall be followed to assure that limited access is  
maintained (e.g., restricted terminals, passwords, etc.).  
(d) A quality assurance representative shall verify screening, qualification, and quality conformance  
inspection records when corrective addenda affect lot jeopardy.  
(3) Control of computerized lot history records:  
(a) All computer lot history records shall have an accurate tape or equivalent backup generated prior to  
lot shipment. Within 3 months of lot shipment, the backup record shall be transferred to a secure  
location to be archived.  
(b) These archived tapes or equivalent media shall be kept for a minimum of 5 years.  
A.4.8.1.2.1 Personnel training and testing. Records shall cover the nature of training or testing given, the date  
thereof by week and length in hours, and the group(s) of personnel given work training and testing. Records are  
required only for product-related training and testing as distinguished from safety, first aid, etc.  
A.4.8.1.2.1.1 Training of operators and inspectors. All critical processes and production inspection shall be  
performed by personnel who have been trained by the manufacturer to perform their assignment task in accordance  
with manufacturer's in-house standards, including a formal training (e.g., classroom or on the job training supervised  
by a certified trainer) and test procedure to assure the proficiency of each individual. Each individual shall be  
retested or retrained at the end of a designated period or when personnel performance indicates poor proficiency.  
Personnel shall not be used in critical processes or inspections until the required level of proficiency has been  
demonstrated.  
A.4.8.1.2.2 Inspection operations. Records of inspection operations shall cover the tests or inspections made, the  
materials group (lot, batch, etc.) inspected, the controlling documentation, the date of completion of inspection, the  
amount of material tested, and acceptance, rejection, or other final disposition of the material.  
A.4.8.1.2.3 Failure and defect reports and analyses. Records of failed or defective devices shall cover the source  
from which each device was received, the test or operation during which failure occurred or defects were observed,  
and prior testing or screening history of the device, the date of receipt, and the disposition of the device. Records of  
failure and defect analyses shall cover the nature of the reported failure or defect (failure or defect mode), verification  
of the failure or defect, the nature of any device discrepancies which were found during analysis (failure or defect  
mechanism), assignment of the failure-activating cause if possible, the date of completion of the analysis,  
identification of the group performing the analysis, disposition of the device after analysis, and the distribution of the  
record. The record shall also treat the relationship of observed failure or defect modes in related lots or devices and,  
where applicable, corrective action taken as a result of the findings.  
A.4.8.1.2.4 Initial documentation and subsequent changes in design, materials, or processing. Records shall  
cover the initial documentation and all changes with the date upon which each change in design, materials, or  
processing becomes effective for devices intended to be submitted for quality conformance inspection under this  
specification, the documents authorizing and implementing the change, and identification of the first production and  
quality conformance inspection lot(s) (as applicable) within which product incorporating the change is included shall  
be maintained when the change requires notification of the qualifying activity (see A.3.4.2).  
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