FDA Inspection 950368 — ImaCor Inc.
The FDA completed an inspection of ImaCor Inc. on November 23, 2015 in Jericho, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- November 23, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Jericho, NY (United States)