FDA Inspection 752368 — Sofradim Production

Sofradim Production — FEI 3003521774

The FDA completed an inspection of Sofradim Production on Nov 7, 2011 in Trevoux. 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
Nov 7, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Trevoux (France)

Citations

IDCFRDescription
1472121 CFR 820.70(g)(2)Periodic equipment inspections

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