# The H.T. Hackney Company, Indianapolis, IN – FDA Inspections

Source: https://www.keypedia.com/companies/the-ht-hackney-company/b418b24b-277f-49d2-8d05-db75e41ffddb

> Inspection records and compliance data for The H.T. Hackney Company in Indianapolis, Indiana. 6 FDA inspections on record, last inspected September 23, 2026.

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## Details

- Name: The H.T. Hackney Company
- FEI Number: 3001134761
- Address Line 1: 9420a E 33rd St
- City: Indianapolis
- State: Indiana
- Zip Code: 46235
- Country Name: United States
- Address: 9420a E 33rd St, Indianapolis, Indiana 46235, United States
- Country: United States

## Related Documents

- FDA Inspection 1337118 - The H.T. Hackney Company - 2026-09-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 23, 2026
- FDA Inspection 1337118 - The H.T. Hackney Company - 2026-09-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 23, 2026
- FDA Inspection 1337118 - The H.T. Hackney Company - 2026-09-23 — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 23, 2026
- [FDA Inspection 1337118 - The H.T. Hackney Company - 2026-09-23](https://www.keypedia.com/records/fda_inspections/the-ht-hackney-company/affb1b13-436a-4b3d-ab5a-58d1eb9a37a2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 23, 2026
- FDA Inspection 1249334 - The H.T. Hackney Company - 2024-07-23 — source: FDA, date: July 23, 2024
- [FDA Inspection 1096330 - The H.T. Hackney Company - 2019-06-07](https://www.keypedia.com/records/fda_inspections/the-ht-hackney-company/1c84e68c-68c7-4647-a607-603ab1ba070f) — classification: No Action Indicated (NAI), source: FDA, date: June 7, 2019
- FDA Inspection 805386 - The H.T. Hackney Company - 2012-04-10 — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2012
- FDA Inspection 772019 - The H.T. Hackney Company - 2012-03-14 — classification: No Action Indicated (NAI), source: FDA, date: March 14, 2012
- FDA Inspection 563641 - The H.T. Hackney Company - 2009-01-22 — classification: No Action Indicated (NAI), source: FDA, date: January 22, 2009

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