998381

Biomet, Inc. — FEI 1825034

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
November 22, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Warsaw, IN (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1472221 CFR 820.40Procedures not adequately established or maintained
237121 CFR 820.30(a)Design control - no procedures
311121 CFR 820.70(f)Buildings
311921 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
312021 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
313021 CFR 820.100(a)Lack of or inadequate procedures
326321 CFR 820.250(b)Sampling plans
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
328521 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
368021 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
54121 CFR 820.70(c)Environmental control Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation