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FDA Inspection 1028624 — Ernest Mazzaferri, MD

Ernest Mazzaferri, MD — FEI 3012934320

The FDA completed an inspection of Ernest Mazzaferri, MD on Sep 29, 2017 in Columbus, OH. 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
Sep 29, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Columbus, OH (United States)

Additional details

Clinical Investigator (CI)

Facility

FDA data resources

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