FDA Inspection 840684 — Gyrus ACMI, Inc.

Gyrus ACMI, Inc. — FEI 3004450998

The FDA completed an inspection of Gyrus ACMI, Inc. on Jun 21, 2013 in Redmond, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 21, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Redmond, WA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures