FDA Inspection 874558 — ACUTRONIC Medical Systems AG

ACUTRONIC Medical Systems AG — FEI 3005929038

The FDA completed an inspection of ACUTRONIC Medical Systems AG on April 10, 2014 in Hirzel. 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
April 10, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Hirzel (Switzerland)