FDA Inspection 716902 — ORCHID Orthopedic Solutions, Ltd.

ORCHID Orthopedic Solutions, Ltd. — FEI 3010089671

The FDA completed an inspection of ORCHID Orthopedic Solutions, Ltd. on January 27, 2011 in Sheffield. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 27, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Sheffield (United Kingdom)