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FDA Inspection 1019700 — Simtra Deutschland GmbH

Simtra Deutschland GmbH — FEI 3002806419

The FDA completed an inspection of Simtra Deutschland GmbH on June 27, 2017 in Halle (Westf.). 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
June 27, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Halle (Westf.) (Germany)

Facility

Other inspections at this facility

  • 1283802 (OAI Fri Sep 26 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1206312 (NAI Wed May 03 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1161093 (VAI Wed Jan 29 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1106642 (NAI Tue Sep 03 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1056958 (VAI Thu Jun 14 2018 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources