# UTZ Brands, Inc dba UTZ Quality Foods LLC, Grand Rapids, MI – FDA Inspections

Source: https://www.keypedia.com/companies/utz-brands-inc-dba-utz-quality-foods-llc/1ef7d099-b9df-462c-9430-ae70306b104b

> Inspection records and compliance data for UTZ Brands, Inc dba UTZ Quality Foods LLC in Grand Rapids, Michigan. 4 FDA inspections on record, 2 Form 483s, last inspected June 29, 2023.

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## Details

- Name: UTZ Brands, Inc dba UTZ Quality Foods LLC
- FEI Number: 3010991720
- Address Line 1: 219 Canton St Sw Ste A
- City: Grand Rapids
- State: Michigan
- Zip Code: 49507
- Country Name: United States
- Address: 219 Canton St Sw Ste A, Grand Rapids, Michigan 49507, United States
- Country: United States

## Related Documents

- [FDA Inspection 1210512 - UTZ Brands, Inc dba UTZ Quality Foods LLC - 2023-06-29](https://www.keypedia.com/records/fda_inspections/utz-brands-inc-dba-utz-quality-foods-llc/30e58501-b07c-4534-9fe1-fd0fbdeeb9f8) — source: FDA, date: June 29, 2023
- [FDA Inspection 1074272 - UTZ Brands, Inc dba UTZ Quality Foods LLC - 2018-12-04](https://www.keypedia.com/records/fda_inspections/utz-brands-inc-dba-utz-quality-foods-llc/566417f9-df11-4beb-907f-dee13e3d39da) — source: FDA, date: December 4, 2018
- FDA Inspection 846344 - UTZ Brands, Inc dba UTZ Quality Foods LLC - 2013-08-30 — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2013
- [FDA Inspection 846344 - UTZ Brands, Inc dba UTZ Quality Foods LLC - 2013-08-30](https://www.keypedia.com/records/fda_inspections/utz-brands-inc-dba-utz-quality-foods-llc/740e9250-5d50-46e8-8b8d-daf1bbbf4b3d) — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2013
- FDA Inspection 846344 - UTZ Brands, Inc dba UTZ Quality Foods LLC - 2013-08-30 — classification: No Action Indicated (NAI), source: FDA, date: August 30, 2013
- [FDA Inspection 753358 - UTZ Brands, Inc dba UTZ Quality Foods LLC - 2011-11-15](https://www.keypedia.com/records/fda_inspections/utz-brands-inc-dba-utz-quality-foods-llc/6a8e7a0b-770e-4e38-850c-cbfd5bcfc283) — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 15, 2011

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