FDA Inspection 774721 — Ludeca, Inc.

Ludeca, Inc. — FEI 1000222229

The FDA completed an inspection of Ludeca, Inc. on Mar 27, 2012 in Doral, 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
Mar 27, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Doral, FL (United States)