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FDA Inspection 1024384 — Ferndale Laboratories, Inc.

Ferndale Laboratories, Inc. — FEI 1811212

The FDA completed an inspection of Ferndale Laboratories, Inc. on August 2, 2017 in Ferndale, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 2, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Ferndale, MI (United States)

Facility

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  • 1300752 (VAI Fri Feb 27 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1163686 (VAI Fri Mar 04 2022 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))

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