FDA Inspection 1162046 — Radformation Inc.

Radformation Inc. — FEI 3013410552

The FDA completed an inspection of Radformation Inc. on Dec 17, 2021 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
Dec 17, 2021
Fiscal Year
2022
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.