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FDA Inspection 1015851 — Bentley Laboratories LLC

Bentley Laboratories LLC — FEI 2244819

The FDA completed an inspection of Bentley Laboratories LLC on June 9, 2017 in Edison, NJ. 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
June 9, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Edison, NJ (United States)

Facility

Other inspections at this facility

  • 1280817 (OAI Fri Mar 27 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1177681 (VAI Wed Aug 17 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 891860 (VAI Tue Sep 02 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 760764 (VAI Mon Jan 30 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 628446 (VAI Tue Nov 17 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources