FDA Inspection 571542 — Sofradim Production

Sofradim Production — FEI 3003521774

The FDA completed an inspection of Sofradim Production on Jan 22, 2009 in Trevoux. 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
Jan 22, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Trevoux (France)

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