FDA Inspection 1092889 — Sirtex Germany Manufacturing GmbH
The FDA completed an inspection of Sirtex Germany Manufacturing GmbH on April 25, 2019 in Frankfurt Am Main. 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
- April 25, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Frankfurt Am Main (Germany)
Additional Details
Postmarket Audit Inspections