FDA Inspection 1018613 — DC ELEKTRONIK AB
The FDA completed an inspection of DC ELEKTRONIK AB on Feb 8, 2017 in Staffanstorp. 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
- Feb 8, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Staffanstorp (Sweden)