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FDA Inspection 1015439 — Judith Baumhauer, MD

Judith Baumhauer, MD — FEI 3013253458

The FDA completed an inspection of Judith Baumhauer, MD on May 31, 2017 in Rochester, NY. 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
May 31, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Rochester, NY (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.