FDA Inspection 1049402 — BioAgilytix

BioAgilytix — FEI 3013196052

The FDA completed an inspection of BioAgilytix on March 2, 2018 in Hamburg. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 2, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Hamburg (Germany)

Additional Details

Bioanalytical BA/BE