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FDA Inspection 824219 — Exxonmobil Product Solutions Company

Exxonmobil Product Solutions Company — FEI 2313361

The FDA completed an inspection of Exxonmobil Product Solutions Company on March 21, 2013 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
March 21, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Baton Rouge, LA (United States)

Facility

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FDA data resources