764312

Oertel Medical GmbH — FEI 3002809480

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
January 27, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Tuttlingen (Germany)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
1472221 CFR 820.40Procedures not adequately established or maintained
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
311721 CFR 820.70(i)Software validation for automated processes
313021 CFR 820.100(a)Lack of or inadequate procedures
316021 CFR 820.184Lack of or inadequate DHR procedures
328521 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
333121 CFR 820.181DMR - not or inadequately maintained
369621 CFR 820.100(b)Documentation
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures