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FDA Inspection 1031348 — Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)

Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) — FEI 3005987757

The FDA completed an inspection of Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) on November 2, 2017 in Ravensburg. 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 2, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Ravensburg (Germany)

Facility

Other inspections at this facility

  • 1253708 (VAI Fri Jul 21 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1205732 (NAI Wed Apr 19 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1155760 (VAI Mon Jul 20 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1060641 (NAI Tue Jun 12 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 981825 (NAI Tue Jul 26 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources