FDA Inspection 923719 — Fulwell, LLC

Fulwell, LLC — FEI 3010131466

The FDA completed an inspection of Fulwell, LLC on Apr 23, 2015 in Miami, 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
Apr 23, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Miami, FL (United States)