FDA Inspection 676409 — ACUTE Innovations LLC

ACUTE Innovations LLC — FEI 3005670412

The FDA completed an inspection of ACUTE Innovations LLC on August 19, 2010 in Hillsboro, OR. 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
August 19, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Hillsboro, OR (United States)