FDA Inspection 741221 — Cagenix Inc.

Cagenix Inc. — FEI 3007273295

The FDA completed an inspection of Cagenix Inc. on August 16, 2011 in Memphis, TN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
August 16, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Memphis, TN (United States)