FDA Inspection 1087247 — STRATEC SE
The FDA completed an inspection of STRATEC SE on April 18, 2019 in Birkenfeld. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- April 18, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Birkenfeld (Germany)
Additional Details
Postmarket Audit Inspections