FDA Inspection 563042 — Viatek Consumer Products Group, Inc.
The FDA completed an inspection of Viatek Consumer Products Group, Inc. on January 27, 2009 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
- January 27, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Chattanooga, TN (United States)