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FDA Inspection 1068201 — 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 September 27, 2018 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
September 27, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
North Chesterfield, VA (United States)

Facility

Other inspections at this facility

  • 1239230 (VAI Fri May 10 2024 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