FDA Inspection 1096292 — Detectamet, Inc.

Detectamet, Inc. — FEI 3011631224

The FDA completed an inspection of Detectamet, Inc. on July 11, 2019 in Richmond, VA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 11, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Richmond, VA (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures