FDA Inspection 1310504 — Omnivium Pharmaceuticals LLC

Omnivium Pharmaceuticals LLC — FEI 3021958998

The FDA completed an inspection of Omnivium Pharmaceuticals LLC on Mar 27, 2026 in Rahway, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 27, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Rahway, NJ (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

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