FDA Inspection 974405 — ANTHOGYR SAS

ANTHOGYR SAS — FEI 4224

The FDA completed an inspection of ANTHOGYR SAS on June 2, 2016 in Sallanches. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 5 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
June 2, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Sallanches (France)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
54621 CFR 820.75(a)Lack of or inadequate process validation