FDA Inspection 1099565 — Arrowhead Healthcare Supply

Arrowhead Healthcare Supply — FEI 3007639246

The FDA completed an inspection of Arrowhead Healthcare Supply on July 1, 2019 in Duluth, MN. 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
July 1, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Duluth, MN (United States)