FDA Inspection 949043 — Dilon Technologies France SAS
The FDA completed an inspection of Dilon Technologies France SAS on Oct 29, 2015 in Saint-Priest. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 29, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Saint-Priest (France)