FDA inspection

Exxonmobil Product Solutions Company: FDA inspection ending Mar 21, 2013

FDA inspection 824219 · Voluntary Action Indicated (VAI) · Baton Rouge, LA

Key facts

Inspection ID 824219
Firm Exxonmobil Product Solutions Company
FEI number 2313361
Address 4999 Scenic Hwy
City Baton Rouge
State LA
ZIP 70805
Country United States
Fiscal year 2013
Inspection end date Mar 21, 2013
Classification Voluntary Action Indicated (VAI)
Project area Drug Quality Assurance
Product type Drugs

At a glance

  • None Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • Yes Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

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