FDA Inspection 740989 — Diagnostica Stago

Diagnostica Stago — FEI 3002806856

The FDA completed an inspection of Diagnostica Stago on Jul 7, 2011 in Franconville. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 7, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Franconville (France)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
316821 CFR 820.198(a)Complaints