FDA Inspection 1182276 — Vitalgo, Inc.

Vitalgo, Inc. — FEI 3010034871

The FDA completed an inspection of Vitalgo, Inc. on Oct 27, 2022 in Miramar, FL. 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 27, 2022
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Miramar, FL (United States)