# Kruegermann Pickles Inc. - Inspection Records

Source: https://www.globalkeysolutions.net/companies/kruegermann-pickles-inc/28811805-ff81-42da-a47f-b2507092e05f

> Inspection records and compliance data for Kruegermann Pickles Inc. in Los Angeles, California. Access full analysis and detailed observations.

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## Details

- Name: Kruegermann Pickles Inc.
- FEI Number: 2026482
- City: Los Angeles
- State: California
- Country Name: United States
- Address Line 1: 2824 Gilroy St
- Zip Code: 90039

## Related Documents

- [FDA Inspection 1088713 - Kruegermann Pickles Inc. - 2019-03-22](https://www.globalkeysolutions.net/records/fda_inspections/kruegermann-pickles-inc/0f07eeed-2b3f-4787-a66f-e8fd77ab61b5) — classification: No Action Indicated (NAI), source: FDA, date: March 22, 2019
- [FDA Inspection 1088713 - Kruegermann Pickles Inc. - 2019-03-22](https://www.globalkeysolutions.net/records/fda_inspections/kruegermann-pickles-inc/f640b880-1806-42e5-a87a-03282df64ed1) — classification: No Action Indicated (NAI), source: FDA, date: March 22, 2019
- [FDA Inspection 962202 - Kruegermann Pickles Inc. - 2016-03-02](https://www.globalkeysolutions.net/records/fda_inspections/kruegermann-pickles-inc/403f5d99-46b8-4a50-9587-7bc3722117eb) — classification: No Action Indicated (NAI), source: FDA, date: March 2, 2016
- [FDA Inspection 759623 - Kruegermann Pickles Inc. - 2011-12-21](https://www.globalkeysolutions.net/records/fda_inspections/kruegermann-pickles-inc/04f4185c-da82-4c22-b3f5-8d30ddd7b4f4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 21, 2011
- [FDA Inspection 670775 - Kruegermann Pickles Inc. - 2010-06-30](https://www.globalkeysolutions.net/records/fda_inspections/kruegermann-pickles-inc/cdf7e4d4-c3c0-485f-a640-ffcf66532098) — classification: No Action Indicated (NAI), source: FDA, date: June 30, 2010
- [FDA Inspection 613167 - Kruegermann Pickles Inc. - 2009-09-17](https://www.globalkeysolutions.net/records/fda_inspections/kruegermann-pickles-inc/921c70c9-12f8-4528-95c1-56c96c5b30fb) — classification: No Action Indicated (NAI), source: FDA, date: September 17, 2009

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