# Gilster-Mary Lee Corp. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/gilster-mary-lee-corp/3fc7e666-f61a-4bf2-8ec7-91db098c434b

> Inspection records and compliance data for Gilster-Mary Lee Corp. in Steeleville, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Gilster-Mary Lee Corp.
- FEI Number: 1450740
- City: Steeleville
- State: Illinois
- Country Name: United States
- Address Line 1: 705 N Sparta St
- Zip Code: 62288

## Related Documents

- [FDA Inspection 1090678 - Gilster-Mary Lee Corp. - 2019-03-13](https://www.globalkeysolutions.net/records/fda_inspections/gilster-mary-lee-corp/1ce64314-37aa-454d-8434-eaf374492d84) — classification: No Action Indicated (NAI), source: FDA, date: March 13, 2019
- [FDA Inspection 1090678 - Gilster-Mary Lee Corp. - 2019-03-13](https://www.globalkeysolutions.net/records/fda_inspections/gilster-mary-lee-corp/84f5e1c6-53bd-406d-9650-1d8c6d96a69a) — classification: No Action Indicated (NAI), source: FDA, date: March 13, 2019
- [FDA Inspection 1008015 - Gilster-Mary Lee Corp. - 2017-03-08](https://www.globalkeysolutions.net/records/fda_inspections/gilster-mary-lee-corp/fc4cd604-eac7-4edf-ae24-24488b4eb7db) — classification: No Action Indicated (NAI), source: FDA, date: March 8, 2017
- [FDA Inspection 885468 - Gilster-Mary Lee Corp. - 2014-06-05](https://www.globalkeysolutions.net/records/fda_inspections/gilster-mary-lee-corp/d237a54a-d056-44bb-8792-6a41c28016f5) — classification: No Action Indicated (NAI), source: FDA, date: June 5, 2014
- [FDA Inspection 629951 - Gilster-Mary Lee Corp. - 2009-11-17](https://www.globalkeysolutions.net/records/fda_inspections/gilster-mary-lee-corp/11527b6b-42c0-48b7-95a4-2def39c85326) — classification: No Action Indicated (NAI), source: FDA, date: November 17, 2009
- [FDA Inspection 566221 - Gilster-Mary Lee Corp. - 2009-03-03](https://www.globalkeysolutions.net/records/fda_inspections/gilster-mary-lee-corp/a1e3aefe-b1d0-4549-a851-c0ad00dfd831) — classification: No Action Indicated (NAI), source: FDA, date: March 3, 2009

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