FDA Inspection 1153385 — Wilmington Reproductive Laboratories

Wilmington Reproductive Laboratories — FEI 3014420061

The FDA completed an inspection of Wilmington Reproductive Laboratories on Aug 26, 2021 in Wilmington, 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
Aug 26, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Wilmington, NC (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.