FDA Inspection 914308 — Interlab S.r.l.
The FDA completed an inspection of Interlab S.r.l. on January 29, 2015 in Rome. 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
- January 29, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Rome (Italy)