# Blue Island Phenol LLC - Inspection Records

Source: https://www.keypedia.com/companies/blue-island-phenol-llc/5c6b5b71-5171-472e-b29d-f605c09f8610

> Inspection records and compliance data for Blue Island Phenol LLC in Blue Island, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Blue Island Phenol LLC
- FEI Number: 1419515
- City: Blue Island
- State: Illinois
- Country Name: United States
- Address Line 1: 3350 131st St
- Zip Code: 60406

## Related Documents

- [FDA Inspection 798519 - Blue Island Phenol LLC - 2012-09-27](https://www.keypedia.com/records/fda_inspections/blue-island-phenol-llc/c7b5dc06-a092-4a9f-aaea-a89fcf3d16ce) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 27, 2012
- [FDA Inspection 798519 - Blue Island Phenol LLC - 2012-09-27](https://www.keypedia.com/records/fda_inspections/blue-island-phenol-llc/2dbf02b8-803f-4072-9210-143f234fd3ae) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 27, 2012
- [FDA Inspection 682265 - Blue Island Phenol LLC - 2010-09-29](https://www.keypedia.com/records/fda_inspections/blue-island-phenol-llc/223f4c3a-0a4b-4db0-ae69-f2c495c28915) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 29, 2010
- [FDA Inspection 682265 - Blue Island Phenol LLC - 2010-09-29](https://www.keypedia.com/records/fda_inspections/blue-island-phenol-llc/a1b42acb-9d20-4474-b872-376eeda06a1c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 29, 2010
- [FDA Inspection 557797 - Blue Island Phenol LLC - 2009-04-02](https://www.keypedia.com/records/fda_inspections/blue-island-phenol-llc/90e09e7c-594e-427c-b5cf-4951d5a3da3d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 2, 2009
- [FDA Inspection 557797 - Blue Island Phenol LLC - 2009-04-02](https://www.keypedia.com/records/fda_inspections/blue-island-phenol-llc/9ee6898c-c5da-4aaa-989f-dd9f3cf33ee7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 2, 2009

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