FDA Inspection 635167 — Laboratoires Synth-Innove

Laboratoires Synth-Innove — FEI 3007851715

The FDA completed an inspection of Laboratoires Synth-Innove on Oct 28, 2009 in Paris. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Oct 28, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Paris (France)

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