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FDA Inspection 1227976 — R.D. Laboratories Inc.

R.D. Laboratories Inc. — FEI 1937815

The FDA completed an inspection of R.D. Laboratories Inc. on January 26, 2024 in Washington, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 26, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Washington, MO (United States)

Facility

Other inspections at this facility

  • 1149944 (VAI Fri Aug 27 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 992018 (NAI Wed Nov 02 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 874155 (NAI Tue Apr 08 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 748385 (NAI Wed Oct 05 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 637107 (NAI Wed Jan 06 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources