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FDA Inspection 1082893 — Duane G. Wombolt, MD

Duane G. Wombolt, MD — FEI 3015002910

The FDA completed an inspection of Duane G. Wombolt, MD on Jan 25, 2019 in Norfolk, VA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 25, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Norfolk, VA (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.