FDA Inspection 1116173 — Gyrus ACMI, Inc.

Gyrus ACMI, Inc. — FEI 3011050570

The FDA completed an inspection of Gyrus ACMI, Inc. on January 14, 2020 in Brooklyn Park, MN. 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
January 14, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Brooklyn Park, MN (United States)