FDA Inspection 551252 — iScreen Vision, Inc.
The FDA completed an inspection of iScreen Vision, Inc. on Dec 2, 2008 in Cordova, TN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Dec 2, 2008
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Cordova, TN (United States)