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FDA Inspection 1021856 — Gaetan Deslee, MD

Gaetan Deslee, MD — FEI 3013484188

The FDA completed an inspection of Gaetan Deslee, MD on Jul 6, 2017 in Reims Cedex. 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
Jul 6, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Reims Cedex (France)

Additional details

Clinical Investigator (CI)

Facility

FDA data resources

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