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FDA Inspection 996275 — Catalent Germany Schorndorf GmbH

Catalent Germany Schorndorf GmbH — FEI 3003831171

The FDA completed an inspection of Catalent Germany Schorndorf GmbH on October 26, 2016 in Schorndorf. 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
October 26, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Schorndorf (Germany)

Facility

Other inspections at this facility

  • 1205903 (VAI Thu Mar 17 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1127864 (VAI Fri Feb 14 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1066669 (VAI Fri Sep 21 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 868435 (NAI Fri Feb 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 772774 (NAI Fri Feb 10 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources