# Rio Grande Food Products, Inc., Laurel, MD – FDA Inspections

Source: https://www.keypedia.com/companies/rio-grande-food-products-inc/b138dac6-3c89-478d-9267-4e0befad6efd

> Inspection records and compliance data for Rio Grande Food Products, Inc. in Laurel, Maryland. 7 FDA inspections on record, 1 Form 483, last inspected July 23, 2026.

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## Details

- Name: Rio Grande Food Products, Inc.
- FEI Number: 3008003773
- Address Line 1: 8610 Cherry Ln Ste 51
- City: Laurel
- State: Maryland
- Zip Code: 20707
- Country Name: United States
- Address: 8610 Cherry Ln Ste 51, Laurel, Maryland 20707, United States
- Country: United States

## Related Documents

- FDA Inspection 1327566 - Rio Grande Food Products, Inc. - 2026-07-23 — classification: No Action Indicated (NAI), source: FDA, date: July 23, 2026
- FDA Inspection 1265693 - Rio Grande Food Products, Inc. - 2025-03-14 — source: FDA, date: March 14, 2025
- [FDA Inspection 1229483 - Rio Grande Food Products, Inc. - 2024-04-10](https://www.keypedia.com/records/fda_inspections/rio-grande-food-products-inc/38137a8b-e58e-4553-927b-9d36a3773fe0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2024
- [FDA Inspection 1201353 - Rio Grande Food Products, Inc. - 2023-03-31](https://www.keypedia.com/records/fda_inspections/rio-grande-food-products-inc/032f753c-f8db-4905-9c2f-dda62984bb13) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 31, 2023
- FDA Inspection 1023117 - Rio Grande Food Products, Inc. - 2017-08-23 — source: FDA, date: August 23, 2017
- FDA Inspection 831408 - Rio Grande Food Products, Inc. - 2013-04-30 — classification: No Action Indicated (NAI), source: FDA, date: April 30, 2013
- [FDA Inspection 781748 - Rio Grande Food Products, Inc. - 2012-05-09](https://www.keypedia.com/records/fda_inspections/rio-grande-food-products-inc/b512a9d2-be27-4386-9b81-69b4d954b91a) — classification: No Action Indicated (NAI), source: FDA, date: May 9, 2012
- FDA Inspection 781748 - Rio Grande Food Products, Inc. - 2012-05-09 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 9, 2012

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