FDA Inspection 1005870 — Michelson Diagnostics Ltd
The FDA completed an inspection of Michelson Diagnostics Ltd on Feb 2, 2017 in Maidstone. 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 2, 2017
- Fiscal Year
- 2017
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Maidstone (United Kingdom)