FDA Inspection 1147778 — HRF, Inc

HRF, Inc — FEI 1053497

The FDA completed an inspection of HRF, Inc on July 27, 2021 in Raleigh, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 27, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Raleigh, NC (United States)

Citations

IDCFRDescription
1808021 CFR 630.10(e)Medical History Interview