FDA Inspection 1026655 — Flowaid Medical Technologies Corp

Flowaid Medical Technologies Corp — FEI 3013411719

The FDA completed an inspection of Flowaid Medical Technologies Corp on August 29, 2017 in New York, 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
August 29, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
New York, NY (United States)