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FDA Inspection 1026806 — NAMSA

NAMSA — FEI 3004495705

The FDA completed an inspection of NAMSA on September 15, 2017 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
September 15, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Chasse-Sur-Rhone (France)

Facility

Other inspections at this facility

  • 1084597 (VAI Wed Mar 27 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 904618 (VAI Wed Jun 11 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 788447 (NAI Thu Apr 05 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 683802 (NAI Wed Mar 31 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources