FDA Inspection 621576 — Ahold Usa

Ahold Usa — FEI 3006470953

The FDA completed an inspection of Ahold Usa on September 14, 2009 in Quincy, MA. 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
September 14, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Quincy, MA (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)