FDA Inspection 1209339 — Annex Medical, Inc.

Annex Medical, Inc. — FEI 2183873

The FDA completed an inspection of Annex Medical, Inc. on June 9, 2023 in Minnetonka, MN. 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
June 9, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Minnetonka, MN (United States)

Citations

IDCFRDescription
310821 CFR 820.70(e)Contamination control, Lack of or inadequate procedures
312021 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
313021 CFR 820.100(a)Lack of or inadequate procedures