# Kraft Heinz Company (NYSE: KHC), Winchester, VA – FDA Inspections

Source: https://www.keypedia.com/companies/kraft-heinz-company/2d26fd58-2577-4427-99aa-ccbc5b462c43

> Inspection records and compliance data for Kraft Heinz Company in Winchester, Virginia. 7 FDA inspections on record, last inspected January 29, 2025. Publicly traded as NYSE: KHC.

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## Details

- Name: Kraft Heinz Company
- FEI Number: 1000123185
- Address Line 1: 220 Park Center Dr
- City: Winchester
- State: Virginia
- Zip Code: 22603
- Country Name: United States
- Address: 220 Park Center Dr, Winchester, Virginia 22603, United States
- Country: United States

## Stock

- Stock ticker: KHC
- Exchange: NYSE
- Share price: $25.32
- Market cap: $30.0B
- Price as of: November 6, 2026

## Related Documents

- FDA Inspection 1273630 - Kraft Heinz Company - 2025-01-29 — source: FDA, date: January 29, 2025
- FDA Inspection 1109898 - Kraft Heinz Company - 2019-07-18 — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2019
- FDA Inspection 1109898 - Kraft Heinz Company - 2019-07-18 — classification: No Action Indicated (NAI), source: FDA, date: July 18, 2019
- FDA Inspection 1030236 - Kraft Heinz Company - 2017-08-08 — classification: No Action Indicated (NAI), source: FDA, date: August 8, 2017
- FDA Inspection 985557 - Kraft Heinz Company - 2016-04-12 — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2016
- FDA Inspection 857350 - Kraft Heinz Company - 2013-12-04 — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2013
- FDA Inspection 857350 - Kraft Heinz Company - 2013-12-04 — classification: No Action Indicated (NAI), source: FDA, date: December 4, 2013
- FDA Inspection 817075 - Kraft Heinz Company - 2013-01-10 — classification: No Action Indicated (NAI), source: FDA, date: January 10, 2013
- FDA Inspection 556101 - Kraft Heinz Company - 2009-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2009
- FDA Inspection 556101 - Kraft Heinz Company - 2009-01-13 — classification: No Action Indicated (NAI), source: FDA, date: January 13, 2009

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