# Darigold Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/darigold-inc/ab961d86-9f46-4502-8ae8-ba9da345bf23

> Inspection records and compliance data for Darigold Inc in Sunnyside, Washington. Access full analysis and detailed observations.

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## Details

- Name: Darigold Inc
- FEI Number: 1000151020
- City: Sunnyside
- State: Washington
- Country Name: United States
- Address Line 1: 400 Alexander Rd
- Zip Code: 98944

## Related Documents

- [FDA Inspection 1250629 - Darigold Inc - 2024-09-12](https://www.globalkeysolutions.net/records/fda_inspections/darigold-inc/a1d09aaa-1c9f-401c-953d-c6e7628396e6) — source: FDA, date: September 12, 2024
- [FDA Inspection 1250629 - Darigold Inc - 2024-09-12](https://www.globalkeysolutions.net/records/fda_inspections/darigold-inc/1e9e2089-7776-40e3-b0ff-af096f60ec58) — source: FDA, date: September 12, 2024
- [FDA Inspection 1250629 - Darigold Inc - 2024-09-12](https://www.globalkeysolutions.net/records/fda_inspections/darigold-inc/def98b96-f22a-44ea-ae37-da3c5f5bea2d) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2024
- [FDA Inspection 1250629 - Darigold Inc - 2024-09-12](https://www.globalkeysolutions.net/records/fda_inspections/darigold-inc/7cf324e5-2e22-472a-a3d8-240b2d886371) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2024
- [FDA Inspection 1250629 - Darigold Inc - 2024-09-12](https://www.globalkeysolutions.net/records/fda_inspections/darigold-inc/3cacbfc7-d03e-4a64-9442-8b793ae5d2ce) — classification: No Action Indicated (NAI), source: FDA, date: September 12, 2024
- [FDA Inspection 889978 - Darigold Inc - 2014-08-01](https://www.globalkeysolutions.net/records/fda_inspections/darigold-inc/d59bf3bf-2589-4bfc-ac3e-a1dce2c09576) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 1, 2014
- [FDA Inspection 847220 - Darigold Inc - 2013-08-06](https://www.globalkeysolutions.net/records/fda_inspections/darigold-inc/a50dc536-dc47-47c5-8df8-dc42723957fe) — classification: No Action Indicated (NAI), source: FDA, date: August 6, 2013

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