FDA Inspection 978527 — Sandoz GmbH
The FDA completed an inspection of Sandoz GmbH on June 30, 2016 in Kundl. 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
- June 30, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kundl (Austria)