FDA Inspection 1079344 — Yohann Loriot, M.D.

Yohann Loriot, M.D. — FEI 3014834015

The FDA completed an inspection of Yohann Loriot, M.D. on Jan 17, 2019 in Villejuif Cedex. 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
Jan 17, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Villejuif Cedex (France)

Additional details

Clinical Investigator (CI)

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