# Abbott Laboratories (NYSE: ABT), Columbus, OH – FDA Inspections

Source: https://www.keypedia.com/companies/abbott-laboratories/f16ac8d3-6abf-4375-a2ff-6db65336ef50

> Inspection records and compliance data for Abbott Laboratories in Columbus, Ohio. 13 FDA inspections on record, last inspected July 22, 2026. Publicly traded as NYSE: ABT.

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## Details

- Name: Abbott Laboratories
- FEI Number: 1000136098
- Address Line 1: 625 Cleveland Ave
- City: Columbus
- State: Ohio
- Zip Code: 43215
- Country Name: United States
- Address: 625 Cleveland Ave, Columbus, Ohio 43215, United States
- Country: United States

## Stock

- Stock ticker: ABT
- Exchange: NYSE
- Share price: $113.74
- Market cap: $197.0B
- Price as of: November 6, 2026

## Related Documents

- FDA Inspection 1325158 - Abbott Laboratories - 2026-07-22 — source: FDA, date: July 22, 2026
- FDA Inspection 1196650 - Abbott Laboratories - 2023-01-19 — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2023
- FDA Inspection 1196650 - Abbott Laboratories - 2023-01-19 — classification: No Action Indicated (NAI), source: FDA, date: January 19, 2023
- FDA Inspection 1144653 - Abbott Laboratories - 2021-03-16 — classification: No Action Indicated (NAI), source: FDA, date: March 16, 2021
- FDA Inspection 979820 - Abbott Laboratories - 2016-07-15 — classification: No Action Indicated (NAI), source: FDA, date: July 15, 2016
- FDA Inspection 941358 - Abbott Laboratories - 2015-09-11 — classification: No Action Indicated (NAI), source: FDA, date: September 11, 2015
- FDA Inspection 897113 - Abbott Laboratories - 2014-09-25 — classification: No Action Indicated (NAI), source: FDA, date: September 25, 2014
- FDA Inspection 848382 - Abbott Laboratories - 2013-09-20 — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2013
- FDA Inspection 800067 - Abbott Laboratories - 2012-09-21 — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2012
- FDA Inspection 760685 - Abbott Laboratories - 2011-12-27 — classification: No Action Indicated (NAI), source: FDA, date: December 27, 2011

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