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FDA Inspection 1239230 — FUJIFILM Wako Chemicals U.S.A. Corporation

FUJIFILM Wako Chemicals U.S.A. Corporation — FEI 1627434

The FDA completed an inspection of FUJIFILM Wako Chemicals U.S.A. Corporation on May 10, 2024 in North Chesterfield, VA. 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
May 10, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Blood and Blood Products
Location
North Chesterfield, VA (United States)

Facility

Other inspections at this facility

  • 1068201 (VAI Thu Sep 27 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1016253 (VAI Wed Apr 12 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 907434 (NAI Fri May 23 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 719926 (VAI Thu Mar 03 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources