FDA Inspection 1110707 — Trigen Laboratories

Trigen Laboratories — FEI 3009428989

The FDA completed an inspection of Trigen Laboratories on November 15, 2019 in Alpharetta, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 15, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Alpharetta, GA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures
63021 CFR 803.17Lack of Written MDR Procedures