FDA Inspection 873595 — MKL DIAGNOSTICS AB
The FDA completed an inspection of MKL DIAGNOSTICS AB on March 25, 2014 in Sollentuna. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI) (OAI)
- End Date
- March 25, 2014
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Sollentuna (Sweden)