FDA Inspection 680877 — Viper Technologies, LLC
The FDA completed an inspection of Viper Technologies, LLC on September 17, 2010 in Portland, OR. 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 17, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Portland, OR (United States)