FDA Inspection 1165285 — Renalytix AI, Inc.

Renalytix AI, Inc. — FEI 3018739912

The FDA completed an inspection of Renalytix AI, Inc. on Mar 1, 2022 in Long Island City, 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
Mar 1, 2022
Fiscal Year
2022
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Long Island City, NY (United States)

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