FDA Inspection 1010222 — HEMOGENYX LLC

HEMOGENYX LLC — FEI 3011400028

The FDA completed an inspection of HEMOGENYX LLC on May 4, 2017 in Brooklyn, NY. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 4, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Brooklyn, NY (United States)