FDA Inspection 963380 — HRF, Inc

HRF, Inc — FEI 1053497

The FDA completed an inspection of HRF, Inc on Mar 18, 2016 in Raleigh, NC. 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
Mar 18, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Raleigh, NC (United States)

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