FDA Inspection 1239408 — Cagenix Inc.

Cagenix Inc. — FEI 3007273295

The FDA completed an inspection of Cagenix Inc. on April 25, 2024 in Memphis, TN. 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
April 25, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Memphis, TN (United States)