# Sbl Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/sbl-inc/656f415b-77bc-4675-b70a-08ac96d30f73

> Inspection records and compliance data for Sbl Inc. in Chicago, Illinois. Access full analysis and detailed observations.

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## Details

- Name: Sbl Inc.
- FEI Number: 2000015629
- City: Chicago
- State: Illinois
- Country Name: United States
- Address Line 1: 1001 W 45th St
- Zip Code: 60609

## Related Documents

- [FDA Inspection 1083572 - Sbl Inc. - 2019-03-14](https://www.globalkeysolutions.net/records/fda_inspections/sbl-inc/cbb940b4-92fe-41a6-8411-3b5c6614cc47) — classification: No Action Indicated (NAI), source: FDA, date: March 14, 2019
- [FDA Inspection 1083572 - Sbl Inc. - 2019-03-14](https://www.globalkeysolutions.net/records/fda_inspections/sbl-inc/9d2bd3e6-a07d-429a-bb65-be09911441ac) — classification: No Action Indicated (NAI), source: FDA, date: March 14, 2019
- [FDA Inspection 967755 - Sbl Inc. - 2016-02-12](https://www.globalkeysolutions.net/records/fda_inspections/sbl-inc/13b2586c-f577-4081-b35e-19ac0c8aae3e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 12, 2016
- [FDA Inspection 821670 - Sbl Inc. - 2013-03-06](https://www.globalkeysolutions.net/records/fda_inspections/sbl-inc/0f0f0b0b-cd72-4eab-bb36-c33715f08cd0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 6, 2013
- [FDA Inspection 821670 - Sbl Inc. - 2013-03-06](https://www.globalkeysolutions.net/records/fda_inspections/sbl-inc/8e6a85ae-e329-4618-887a-9c1bb77a66ee) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 6, 2013
- [FDA Inspection 667359 - Sbl Inc. - 2010-06-16](https://www.globalkeysolutions.net/records/fda_inspections/sbl-inc/a2157e65-6e6c-422d-a68d-e3fd2d7e541c) — classification: No Action Indicated (NAI), source: FDA, date: June 16, 2010
- [FDA Inspection 598516 - Sbl Inc. - 2009-08-10](https://www.globalkeysolutions.net/records/fda_inspections/sbl-inc/2cf4d03a-7fcd-41f0-a049-d721884b9af5) — classification: No Action Indicated (NAI), source: FDA, date: August 10, 2009

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