FDA Inspection 1158171 — Birth Tissue Recovery

Birth Tissue Recovery — FEI 3014254014

The FDA completed an inspection of Birth Tissue Recovery on Oct 21, 2021 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
Oct 21, 2021
Fiscal Year
2022
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Raleigh, NC (United States)