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FDA Inspection 937801 — Similasan AG

Similasan AG — FEI 1000110034

The FDA completed an inspection of Similasan AG on July 23, 2015 in Jonen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 23, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Jonen (Switzerland)

Facility

Other inspections at this facility

  • 1204144 (OAI Tue Apr 04 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1028938 (NAI Mon Sep 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 851899 (VAI Fri Sep 13 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 727380 (VAI Fri May 27 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources