# Refresco Beverages North America, Paw Paw, MI – FDA Inspections

Source: https://www.keypedia.com/companies/refresco-beverages-north-america/ee19b8b6-4e04-46cd-9676-538bb4f0ace8

> Inspection records and compliance data for Refresco Beverages North America in Paw Paw, Michigan. 6 FDA inspections on record, last inspected March 04, 2024.

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## Details

- Name: Refresco Beverages North America
- FEI Number: 1826632
- Address Line 1: 38279 W Red Arrow Hwy
- City: Paw Paw
- State: Michigan
- Zip Code: 49079
- Country Name: United States
- Address: 38279 W Red Arrow Hwy, Paw Paw, Michigan 49079, United States
- Country: United States

## Related Documents

- FDA Inspection 1233915 - Refresco Beverages North America - 2024-03-04 — source: FDA, date: March 4, 2024
- FDA Inspection 1096321 - Refresco Beverages North America - 2019-06-12 — classification: No Action Indicated (NAI), source: FDA, date: June 12, 2019
- FDA Inspection 1096321 - Refresco Beverages North America - 2019-06-12 — classification: No Action Indicated (NAI), source: FDA, date: June 12, 2019
- FDA Inspection 906001 - Refresco Beverages North America - 2014-12-03 — classification: No Action Indicated (NAI), source: FDA, date: December 3, 2014
- [FDA Inspection 800573 - Refresco Beverages North America - 2012-09-24](https://www.keypedia.com/records/fda_inspections/refresco-beverages-north-america/09267bc5-2af0-4a3e-93ee-db72bf469b0b) — classification: No Action Indicated (NAI), source: FDA, date: September 24, 2012
- FDA Inspection 648945 - Refresco Beverages North America - 2010-02-25 — classification: No Action Indicated (NAI), source: FDA, date: February 25, 2010
- FDA Inspection 648945 - Refresco Beverages North America - 2010-02-25 — classification: No Action Indicated (NAI), source: FDA, date: February 25, 2010
- FDA Inspection 580624 - Refresco Beverages North America - 2009-05-06 — classification: No Action Indicated (NAI), source: FDA, date: May 6, 2009
- FDA Inspection 580624 - Refresco Beverages North America - 2009-05-06 — classification: No Action Indicated (NAI), source: FDA, date: May 6, 2009

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