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FDA Inspection 1005002 — Frederic E. Martens, MD

Frederic E. Martens, MD — FEI 3013217220

The FDA completed an inspection of Frederic E. Martens, MD on Mar 17, 2017 in Aalst. 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
Mar 17, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Aalst (Belgium)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources

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