# Exxonmobil Product Solutions Company - Inspection Records

Source: https://www.keypedia.com/companies/exxonmobil-product-solutions-company/8e83c4a4-cc31-4bfd-abc9-d6f2df29259f

> Inspection records and compliance data for Exxonmobil Product Solutions Company in Baton Rouge, LA. Access full analysis and detailed observations.

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## Details

- Name: Exxonmobil Product Solutions Company
- FEI Number: 2313361
- City: Baton Rouge
- State: LA
- Country Name: United States
- Address Line 1: 4999 Scenic Hwy
- Zip Code: 70805-3359
- Business Operations: API MANUFACTURE

## Related Documents

- [483 - Exxonmobil Product Solutions Company - 2025-12-11](https://www.keypedia.com/records/483/exxonmobil-product-solutions-company/6260797e-3f8f-4f4d-b8fc-691b5763e5aa) — source: FDA, date: December 11, 2025
- [FDA Inspection 1299690 - Exxonmobil Product Solutions Company - 2025-12-11](https://www.keypedia.com/records/fda_inspections/exxonmobil-product-solutions-company/379515cf-6950-4f69-978d-49b6512752ad) — source: FDA, date: December 11, 2025
- [FDA Inspection 1299690 - Exxonmobil Product Solutions Company - 2025-12-11](https://www.keypedia.com/records/fda_inspections/exxonmobil-product-solutions-company/33ef8115-f694-48ba-a484-20373a0b90a4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 11, 2025
- [EIR - Exxonmobil Product Solutions Company - 2019-12-11](https://www.keypedia.com/records/eir/exxonmobil-product-solutions-company/6fdfc4e2-9e5c-4f04-9b65-b62c17d9e454) — source: FDA, date: December 11, 2019
- [FDA Inspection 1116384 - Exxonmobil Product Solutions Company - 2019-12-11](https://www.keypedia.com/records/fda_inspections/exxonmobil-product-solutions-company/9c4c03af-e29c-405f-be31-25ed2d2537a2) — classification: No Action Indicated (NAI), source: FDA, date: December 11, 2019
- [EIR - Exxonmobil Product Solutions Company - 2018-03-09](https://www.keypedia.com/records/eir/exxonmobil-product-solutions-company/d0ed0a1b-1752-41a6-a17a-10d99b4eb8db) — source: FDA, date: March 9, 2018
- [FDA Inspection 1044898 - Exxonmobil Product Solutions Company - 2018-03-09](https://www.keypedia.com/records/fda_inspections/exxonmobil-product-solutions-company/1d3f7c78-17a3-4302-934d-ad62b069a72c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 9, 2018
- [FDA Inspection 1044898 - Exxonmobil Product Solutions Company - 2018-03-09](https://www.keypedia.com/records/fda_inspections/exxonmobil-product-solutions-company/dcc239c5-0a6d-4af7-a3a1-48caed014a3f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 9, 2018
- [EIR - Exxonmobil Product Solutions Company - 2016-04-21](https://www.keypedia.com/records/eir/exxonmobil-product-solutions-company/88fed02e-9e74-4007-b291-41937d05ce7e) — source: FDA, date: April 21, 2016
- [FDA Inspection 979492 - Exxonmobil Product Solutions Company - 2016-04-21](https://www.keypedia.com/records/fda_inspections/exxonmobil-product-solutions-company/35e6a437-c211-400d-9b5f-f9863dbbcc00) — classification: No Action Indicated (NAI), source: FDA, date: April 21, 2016
- [FDA Inspection 979492 - Exxonmobil Product Solutions Company - 2016-04-21](https://www.keypedia.com/records/fda_inspections/exxonmobil-product-solutions-company/59a376d6-51f8-416d-b6b6-180a24616017) — classification: No Action Indicated (NAI), source: FDA, date: April 21, 2016
- [EIR - Exxonmobil Product Solutions Company - 2013-03-21](https://www.keypedia.com/records/eir/exxonmobil-product-solutions-company/53416370-c6bc-4e98-ac79-1b0ea273f2c5) — source: FDA, date: March 21, 2013
- [FDA Inspection 824219 - Exxonmobil Product Solutions Company - 2013-03-21](https://www.keypedia.com/records/fda_inspections/exxonmobil-product-solutions-company/46c987f7-b9e9-42f7-8cb7-e488b27fdcdb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 21, 2013
- [FDA Inspection 614653 - Exxonmobil Product Solutions Company - 2009-09-17](https://www.keypedia.com/records/fda_inspections/exxonmobil-product-solutions-company/26374f76-b348-4eb5-915e-2bf1944e930b) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2009

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## Related Officers

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