FDA Inspection 731008 — Gyrus ACMI, Inc.

Gyrus ACMI, Inc. — FEI 3004450998

The FDA completed an inspection of Gyrus ACMI, Inc. on Jun 13, 2011 in Redmond, WA. 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
Jun 13, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Redmond, WA (United States)