FDA Inspection 676524 — Skanray Technologies Pvt. Ltd
The FDA completed an inspection of Skanray Technologies Pvt. Ltd on Jun 25, 2010 in Mysore. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jun 25, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Mysore (India)