FDA Inspection 1275315 — FHC, Inc.

FHC, Inc. — FEI 3002250546

The FDA completed an inspection of FHC, Inc. on Jul 10, 2025 in Bowdoin, ME. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 10, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: 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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.