FDA Inspection 992519 — Altergon Italia s.r.l.
The FDA completed an inspection of Altergon Italia s.r.l. on November 9, 2016 in Morra De Sanctis. 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
- November 9, 2016
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Morra De Sanctis (Italy)