FDA Inspection 1026655 — Flowaid Medical Technologies Corp

Flowaid Medical Technologies Corp — FEI 3013411719

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.