FDA Inspection 728118 — ImaCor Inc.

ImaCor Inc. — FEI 3006382185

The FDA completed an inspection of ImaCor Inc. on June 2, 2011 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
June 2, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Jericho, NY (United States)