FDA Inspection 650559 — Sintea Plustek S.P.A.
The FDA completed an inspection of Sintea Plustek S.P.A. on Feb 4, 2010 in Assago. 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
- Feb 4, 2010
- Fiscal Year
- 2010
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Assago (Italy)