FDA Inspection 1014345 — ORCHID Orthopedic Solutions, Ltd.

ORCHID Orthopedic Solutions, Ltd. — FEI 3010089671

The FDA completed an inspection of ORCHID Orthopedic Solutions, Ltd. on May 11, 2017 in Sheffield. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
May 11, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Sheffield (United Kingdom)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.