FDA Inspection 859340 — KMI IMI Group
The FDA completed an inspection of KMI IMI Group on Dec 17, 2013 in Irvine, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Dec 17, 2013
- Fiscal Year
- 2014
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Irvine, CA (United States)