FDA Inspection 1084597 — NAMSA

NAMSA — FEI 3004495705

The FDA completed an inspection of NAMSA on March 27, 2019 in Chasse-Sur-Rhone. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 27, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Chasse-Sur-Rhone (France)