FDA Inspection 716902 — ORCHID Orthopedic Solutions, Ltd.

ORCHID Orthopedic Solutions, Ltd. — FEI 3010089671

The FDA completed an inspection of ORCHID Orthopedic Solutions, Ltd. on Jan 27, 2011 in Sheffield. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection details

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

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