FDA Inspection 1031485 — Ericka P. Simpson, MD

Ericka P. Simpson, MD — FEI 3013739056

The FDA completed an inspection of Ericka P. Simpson, MD on Nov 1, 2017 in Houston, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 1, 2017
Fiscal Year
2018
Product Type
Biologics
Project Area
Bioresearch Monitoring
Location
Houston, TX (United States)

Additional Details

Clinical Investigator (CI)

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