FDA Inspection 1029050 — FootMaxx Inc.
The FDA completed an inspection of FootMaxx Inc. on September 19, 2017 in Roanoke, VA. 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
- September 19, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Roanoke, VA (United States)