FDA Inspection 1211660 — ReCor Medical Inc.

ReCor Medical Inc. — FEI 3010024164

The FDA completed an inspection of ReCor Medical Inc. on July 11, 2023 in Palo Alto, CA. 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
July 11, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Palo Alto, CA (United States)

Additional Details

Sponsor, Contract Research Organization