FDA Inspection 1099236 — Osseolink USA, LLC

Osseolink USA, LLC — FEI 3008802367

The FDA completed an inspection of Osseolink USA, LLC on June 18, 2019 in Fort Washington, PA. 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
June 18, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Fort Washington, PA (United States)