FDA Inspection 1283118 — IVI RMA Of New Jersey

IVI RMA Of New Jersey — FEI 3017585297

The FDA completed an inspection of IVI RMA Of New Jersey on Sep 8, 2025 in Marlton, NJ. 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
Sep 8, 2025
Fiscal Year
2025
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
Location
Marlton, NJ (United States)

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