FDA Inspection 991760 — In2Bones, SAS

In2Bones, SAS — FEI 3010470577

The FDA completed an inspection of In2Bones, SAS on Oct 27, 2016 in Ecully. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 27, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Ecully (France)

Citations

IDCFRDescription
342721 CFR 820.50(a)(2)Supplier oversight

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