FDA Inspection 1181772 — Medivis, Inc.

Medivis, Inc. — FEI 3015536273

The FDA completed an inspection of Medivis, Inc. on October 17, 2022 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
October 17, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
New York, NY (United States)