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FDA Inspection 1043915 — Celltrion Branchburg, LLC

Celltrion Branchburg, LLC — FEI 3002889358

The FDA completed an inspection of Celltrion Branchburg, LLC on March 9, 2018 in Branchburg, 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
March 9, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Branchburg, NJ (United States)

Facility

Other inspections at this facility

  • 1178892 (VAI Thu Aug 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1128945 (OAI Fri Aug 21 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1111276 (OAI Tue Nov 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1029810 (NAI Thu Sep 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 933959 (NAI Fri Jul 10 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources