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FDA Inspection 1031350 — Vetter Pharma Fertigung GmbH & Co. KG

Vetter Pharma Fertigung GmbH & Co. KG — FEI 3002808846

The FDA completed an inspection of Vetter Pharma Fertigung GmbH & Co. KG on November 10, 2017 in Langenargen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 10, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Langenargen (Germany)

Facility

Other inspections at this facility

  • 1205983 (VAI Tue May 24 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1129699 (NAI Fri Sep 13 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1070717 (NAI Fri Sep 21 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1001330 (VAI Tue Apr 26 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 873643 (NAI Thu Feb 20 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources