FDA Inspection 783157 — Athena GTX Inc.

Athena GTX Inc. — FEI 3007413079

The FDA completed an inspection of Athena GTX Inc. on May 24, 2012 in Johnston, IA. 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
May 24, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Johnston, IA (United States)