# K AND B CO., Inc, Gallup, NM – FDA Inspections

Source: https://www.keypedia.com/companies/k-and-b-co-inc/8ce941f9-d77b-4d39-b69a-f369141fcd32

> Inspection records and compliance data for K AND B CO., Inc in Gallup, New Mexico. 5 FDA inspections on record, 3 Form 483s, last inspected March 06, 2025.

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## Details

- Name: K AND B CO., Inc
- FEI Number: 1619025
- Address Line 1: 109 Arnold St
- City: Gallup
- State: New Mexico
- Zip Code: 87301
- Country Name: United States
- Address: 109 Arnold St, Gallup, New Mexico 87301, United States
- Country: United States

## Related Documents

- FDA Inspection 1263178 - K AND B CO., Inc - 2025-03-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 6, 2025
- [FDA Inspection 1263178 - K AND B CO., Inc - 2025-03-06](https://www.keypedia.com/records/fda_inspections/k-and-b-co-inc/47a3b820-1e1a-4916-855e-2bd59c74319d) — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2025
- FDA Inspection 1263178 - K AND B CO., Inc - 2025-03-06 — classification: No Action Indicated (NAI), source: FDA, date: March 6, 2025
- [FDA Inspection 1053926 - K AND B CO., Inc - 2018-05-23](https://www.keypedia.com/records/fda_inspections/k-and-b-co-inc/3259072a-0b38-4952-b90e-04f9c5331621) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 23, 2018
- [FDA Inspection 1014238 - K AND B CO., Inc - 2017-05-15](https://www.keypedia.com/records/fda_inspections/k-and-b-co-inc/b29664af-a427-4164-9814-7706e130f204) — source: FDA, date: May 15, 2017
- [FDA Inspection 879175 - K AND B CO., Inc - 2014-05-20](https://www.keypedia.com/records/fda_inspections/k-and-b-co-inc/cfeac8b9-4f46-4be0-8fa3-c51575597348) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 20, 2014
- FDA Inspection 879175 - K AND B CO., Inc - 2014-05-20 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 20, 2014
- FDA Inspection 700090 - K AND B CO., Inc - 2010-10-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 29, 2010

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