# TBL Inc dba Tabs Limited, Saint Joseph, MO – FDA Inspections

Source: https://www.keypedia.com/companies/tbl-inc-dba-tabs-limited/65b0fd1f-3b44-4581-a1b9-3f4672fab733

> Inspection records and compliance data for TBL Inc dba Tabs Limited in Saint Joseph, Missouri. 8 FDA inspections on record, last inspected August 03, 2026.

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## Details

- Name: TBL Inc dba Tabs Limited
- FEI Number: 3002265489
- Address Line 1: 751 S 4th St
- City: Saint Joseph
- State: Missouri
- Zip Code: 64501
- Country Name: United States
- Address: 751 S 4th St, Saint Joseph, Missouri 64501, United States
- Country: United States

## Related Documents

- FDA Inspection 1329794 - TBL Inc dba Tabs Limited - 2026-08-03 — classification: No Action Indicated (NAI), source: FDA, date: August 3, 2026
- FDA Inspection 1310632 - TBL Inc dba Tabs Limited - 2026-04-01 — classification: No Action Indicated (NAI), source: FDA, date: April 1, 2026
- FDA Inspection 1097861 - TBL Inc dba Tabs Limited - 2019-07-18 — source: FDA, date: July 18, 2019
- [FDA Inspection 1045756 - TBL Inc dba Tabs Limited - 2018-01-22](https://www.keypedia.com/records/fda_inspections/tbl-inc-dba-tabs-limited/181f0c95-049b-4b6c-bd7d-cdefa52fc641) — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2018
- [FDA Inspection 922949 - TBL Inc dba Tabs Limited - 2015-03-06](https://www.keypedia.com/records/fda_inspections/tbl-inc-dba-tabs-limited/171f9a4c-4aa8-47e8-bf6a-49b9127c3126) — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2015
- FDA Inspection 812492 - TBL Inc dba Tabs Limited - 2012-12-31 — classification: No Action Indicated (NAI), source: FDA, date: December 31, 2012
- FDA Inspection 754081 - TBL Inc dba Tabs Limited - 2011-11-16 — classification: No Action Indicated (NAI), source: FDA, date: November 16, 2011
- FDA Inspection 603170 - TBL Inc dba Tabs Limited - 2009-07-24 — classification: No Action Indicated (NAI), source: FDA, date: July 24, 2009
- FDA Inspection 603170 - TBL Inc dba Tabs Limited - 2009-07-24 — classification: No Action Indicated (NAI), source: FDA, date: July 24, 2009

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