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FDA Inspection 597351 — Biotronik SE & Co. KG

Biotronik SE & Co. KG — FEI 3002806500

The FDA completed an inspection of Biotronik SE & Co. KG on July 2, 2009 in Berlin. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 2, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Berlin (Germany)

Additional Details

Postmarket Audit Inspections

Facility

Other inspections at this facility

  • 1022011 (NAI Thu Jun 22 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 965124 (OAI Thu Mar 10 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 847640 (VAI Tue Aug 13 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 742999 (VAI Thu Aug 18 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources