FDA Inspection 1233462 — Chitogen, Inc.

Chitogen, Inc. — FEI 3007788086

The FDA completed an inspection of Chitogen, Inc. on Mar 19, 2024 in Maple Grove, MN. 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
Mar 19, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Maple Grove, MN (United States)

Citations

IDCFRDescription
312721 CFR 820.80(e)Documentation
313021 CFR 820.100(a)Lack of or inadequate procedures