FDA Inspection 1011332 — Viatek Consumer Products Group, Inc.
The FDA completed an inspection of Viatek Consumer Products Group, Inc. on May 9, 2017 in Chattanooga, TN. 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
- May 9, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Chattanooga, TN (United States)