FDA Inspection 1181772 — Medivis, Inc.

Medivis, Inc. — FEI 3015536273

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

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