FDA Inspection 1153385 — Wilmington Reproductive Laboratories

Wilmington Reproductive Laboratories — FEI 3014420061

The FDA completed an inspection of Wilmington Reproductive Laboratories on August 26, 2021 in Wilmington, NC. 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
August 26, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Wilmington, NC (United States)