FDA Inspection 1143584 — ImaCor Inc.

ImaCor Inc. — FEI 3006382185

The FDA completed an inspection of ImaCor Inc. on June 10, 2021 in Jericho, NY. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 10, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Jericho, NY (United States)

Citations

IDCFRDescription
316821 CFR 820.198(a)Complaints
319921 CFR 820.40(a)Document review, approval documentation
63021 CFR 803.17Lack of Written MDR Procedures