FDA Inspection 1030704 — Eagle Laboratories

Eagle Laboratories — FEI 2027619

The FDA completed an inspection of Eagle Laboratories on Dec 5, 2016 in Saint Paul, MN. 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
Dec 5, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Paul, MN (United States)