FDA Inspection 1073154 — Helen L. How MD

Helen L. How MD — FEI 3014699346

The FDA completed an inspection of Helen L. How MD on Nov 9, 2018 in Louisville, KY. 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 9, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Louisville, KY (United States)

Additional Details

Clinical Investigator (CI)

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