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FDA Inspection 1116384 — Exxonmobil Product Solutions Company

Exxonmobil Product Solutions Company — FEI 2313361

The FDA completed an inspection of Exxonmobil Product Solutions Company on December 11, 2019 in Baton Rouge, LA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Veterinary.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 11, 2019
Fiscal Year
2020
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Baton Rouge, LA (United States)

Facility

Other inspections at this facility

  • 1299690 (VAI Thu Dec 11 2025 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