FDA Inspection 1087831 — Medistri SA
The FDA completed an inspection of Medistri SA on Jan 31, 2019 in Domdidier. 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
- Jan 31, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Project Evaluation: Devices
- Location
- Domdidier (Switzerland)
Additional Details
Postmarket Audit Inspections