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FDA Inspection 1050123 — Siegfried Hameln GmbH

Siegfried Hameln GmbH — FEI 3002807877

The FDA completed an inspection of Siegfried Hameln GmbH on April 24, 2018 in Hameln. 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
April 24, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Hameln (Germany)

Facility

Other inspections at this facility

  • 1203347 (VAI Thu Sep 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 987428 (VAI Fri Jul 01 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 887446 (VAI Fri Jul 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 786813 (OAI Thu Jun 14 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 637807 (VAI Mon Nov 09 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources