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FDA Inspection 1039401 — Patheon Manufacturing Services LLC

Patheon Manufacturing Services LLC — FEI 2246315

The FDA completed an inspection of Patheon Manufacturing Services LLC on December 7, 2017 in Ridgefield, 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
December 7, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ridgefield, NJ (United States)

Facility

Other inspections at this facility

  • 1230469 (VAI Thu Jun 13 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1230688 (VAI Mon Mar 18 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1076243 (VAI Mon Dec 17 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 938525 (NAI Wed Aug 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 861702 (VAI Tue Jan 21 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources