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FDA Inspection 1299690 — Exxonmobil Product Solutions Company

Exxonmobil Product Solutions Company — FEI 2313361

The FDA completed an inspection of Exxonmobil Product Solutions Company on December 11, 2025 in Baton Rouge, LA. 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
December 11, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baton Rouge, LA (United States)

Facility

Other inspections at this facility

  • 1116384 (NAI Wed Dec 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1044898 (VAI Fri Mar 09 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 979492 (NAI Thu Apr 21 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 824219 (VAI Thu Mar 21 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 614653 (NAI Thu Sep 17 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources