FDA Inspection 1030243 — James A. Tumlin, MD

James A. Tumlin, MD — FEI 3010185725

The FDA completed an inspection of James A. Tumlin, MD on Sep 22, 2017 in Lawrenceville, GA. 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 22, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Lawrenceville, GA (United States)

Additional Details

Clinical Investigator (CI)

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