FDA Inspection 1232181 — Accugenix LLC

Accugenix LLC — FEI 3002920000

The FDA completed an inspection of Accugenix LLC on March 1, 2024 in Newark, DE. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 1, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Newark, DE (United States)