FDA Inspection 546189 — Accugenix LLC

Accugenix LLC — FEI 3002920000

The FDA completed an inspection of Accugenix LLC on October 31, 2008 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
October 31, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Newark, DE (United States)