FDA Inspection 881413 — Aletha Veenendaal

Aletha Veenendaal — FEI 3010753189

The FDA completed an inspection of Aletha Veenendaal on May 27, 2014 in Almere. 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
May 27, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Almere (Netherlands)

Additional Details

Clinical Investigator (CI)