# AHC Products Inc, Winchester, KY – FDA Inspections

Source: https://www.keypedia.com/companies/ahc-products-inc/4d6352d5-7905-4be6-9151-3c7345e363fe

> Inspection records and compliance data for AHC Products Inc in Winchester, Kentucky. 11 FDA inspections on record, 3 Form 483s, 1 warning letter, last inspected October 23, 2025.

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## Details

- Name: AHC Products Inc
- FEI Number: 3002745172
- Address Line 1: 301 W Broadway St
- City: Winchester
- State: Kentucky
- Zip Code: 40391
- Country Name: United States
- Address: 301 W Broadway St, Winchester, Kentucky 40391, United States
- Country: United States

## Related Documents

- [WARNING_LETTER - AHC Products Inc - 2025-10-23](https://www.keypedia.com/records/warning_letter/ahc-products-inc/807b6fed-b7c5-432e-883f-66ce2b2d9508) — source: FDA, date: October 23, 2025
- [483 - AHC Products Inc - 2025-10-23](https://www.keypedia.com/records/483/ahc-products-inc/82417e0f-b613-4b90-96d4-f14315c9cae4) — source: FDA, date: October 23, 2025
- [FDA Inspection 1289708 - AHC Products Inc - 2025-10-23](https://www.keypedia.com/records/fda_inspections/ahc-products-inc/90f94529-65b1-42a0-9f1a-ee1844d4d300) — source: FDA, date: October 23, 2025
- [483 - AHC Products Inc - 2022-03-29](https://www.keypedia.com/records/483/ahc-products-inc/ceb49afb-7e87-4ba4-98f9-c264d4adab2e) — source: FDA, date: March 29, 2022
- [FDA Inspection 1165684 - AHC Products Inc - 2022-03-29](https://www.keypedia.com/records/fda_inspections/ahc-products-inc/fc93f269-5faf-448a-943b-17e2b43d24bb) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 29, 2022
- [FDA Inspection 1053221 - AHC Products Inc - 2018-05-24](https://www.keypedia.com/records/fda_inspections/ahc-products-inc/46f7b5ee-e0b2-442f-90ae-181009976e40) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 24, 2018
- FDA Inspection 1044869 - AHC Products Inc - 2018-02-02 — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2018
- FDA Inspection 1044869 - AHC Products Inc - 2018-02-02 — classification: No Action Indicated (NAI), source: FDA, date: February 2, 2018
- [FDA Inspection 1019926 - AHC Products Inc - 2016-10-26](https://www.keypedia.com/records/fda_inspections/ahc-products-inc/2e18a122-cb31-4bf8-8f4a-513c0de07bbc) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 26, 2016
- FDA Inspection 866393 - AHC Products Inc - 2014-02-07 — classification: No Action Indicated (NAI), source: FDA, date: February 7, 2014
- FDA Inspection 866393 - AHC Products Inc - 2014-02-07 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 7, 2014
- [FDA Inspection 788210 - AHC Products Inc - 2012-07-02](https://www.keypedia.com/records/fda_inspections/ahc-products-inc/935a39e6-3b4e-4873-9908-356b4bea461d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 2, 2012
- FDA Inspection 741065 - AHC Products Inc - 2011-04-28 — classification: No Action Indicated (NAI), source: FDA, date: April 28, 2011

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