FDA Inspection 885248 — Athena GTX Inc.

Athena GTX Inc. — FEI 3007413079

The FDA completed an inspection of Athena GTX Inc. on Jun 27, 2014 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
Jun 27, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Johnston, IA (United States)