FDA Inspection 1005880 — Storz Medical, AG

Storz Medical, AG — FEI 3002808188

The FDA completed an inspection of Storz Medical, AG on Feb 10, 2017 in Tagerwilen. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 10, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Tagerwilen (Switzerland)

Additional Details

Postmarket Audit Inspections

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