FDA Inspection 760707 — iScreen Vision, Inc.
The FDA completed an inspection of iScreen Vision, Inc. on December 21, 2011 in Cordova, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- December 21, 2011
- Fiscal Year
- 2012
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Cordova, TN (United States)