FDA Inspection 937301 — Orchid Orthopedic Solutions Oregon, Inc.

Orchid Orthopedic Solutions Oregon, Inc. — FEI 3009848551

The FDA completed an inspection of Orchid Orthopedic Solutions Oregon, Inc. on July 29, 2015 in Oregon City, OR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 29, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Oregon City, OR (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures