FDA Inspection 1040890 — Stephanie Shaw, M.D.

Stephanie Shaw, M.D. — FEI 3013858549

The FDA completed an inspection of Stephanie Shaw, M.D. on Dec 18, 2017 in Round Rock, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 18, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Round Rock, TX (United States)

Additional Details

Clinical Investigator (CI)

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