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FDA Inspection 1091172 — Charles River Laboratories, Inc.

Charles River Laboratories, Inc. — FEI 1053022

The FDA completed an inspection of Charles River Laboratories, Inc. on May 17, 2019 in Charleston, SC. 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 17, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Charleston, SC (United States)

Facility

Other inspections at this facility

  • 1309514 (VAI Fri Mar 27 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1120385 (NAI Tue Aug 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 961187 (VAI Wed Jan 13 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876149 (NAI Thu Apr 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 819221 (VAI Tue Jan 15 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources