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FDA Inspection 1300752 — Ferndale Laboratories, Inc.

Ferndale Laboratories, Inc. — FEI 1811212

The FDA completed an inspection of Ferndale Laboratories, Inc. on February 27, 2026 in Ferndale, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 27, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ferndale, MI (United States)

Facility

Other inspections at this facility

  • 1317968 (NAI Wed May 20 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1163686 (VAI Fri Mar 04 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1024384 (NAI Wed Aug 02 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1005288 (VAI Fri Feb 03 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 924621 (VAI Fri Apr 24 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources