FDA Inspection 1275315 — FHC, Inc.

FHC, Inc. — FEI 3002250546

The FDA completed an inspection of FHC, Inc. on July 10, 2025 in Bowdoin, ME. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 10, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Bowdoin, ME (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
319821 CFR 820.40(b)Document changes, review and approval, communication