# Sunny Delight Beverages Company, Dayton, NJ – FDA Inspections

Source: https://www.keypedia.com/companies/sunny-delight-beverages-company/f21c1e6a-82c9-4972-9e53-8d92ecfec9f7

> Inspection records and compliance data for Sunny Delight Beverages Company in Dayton, New Jersey. 5 FDA inspections on record, last inspected August 23, 2021.

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## Details

- Name: Sunny Delight Beverages Company
- FEI Number: 2241582
- Address Line 1: 10 Corn Rd
- City: Dayton
- State: New Jersey
- Zip Code: 08810
- Country Name: United States
- Address: 10 Corn Rd, Dayton, New Jersey 08810, United States
- Country: United States

## Related Documents

- FDA Inspection 1150562 - Sunny Delight Beverages Company - 2021-08-23 — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2021
- FDA Inspection 1150562 - Sunny Delight Beverages Company - 2021-08-23 — classification: No Action Indicated (NAI), source: FDA, date: August 23, 2021
- FDA Inspection 1046591 - Sunny Delight Beverages Company - 2018-03-12 — classification: No Action Indicated (NAI), source: FDA, date: March 12, 2018
- FDA Inspection 909230 - Sunny Delight Beverages Company - 2015-01-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 8, 2015
- FDA Inspection 909230 - Sunny Delight Beverages Company - 2015-01-08 — classification: No Action Indicated (NAI), source: FDA, date: January 8, 2015
- [FDA Inspection 793214 - Sunny Delight Beverages Company - 2012-08-08](https://www.keypedia.com/records/fda_inspections/sunny-delight-beverages-company/e728be7d-795c-43dd-81d9-8e904a3e08b0) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 8, 2012
- FDA Inspection 793214 - Sunny Delight Beverages Company - 2012-08-08 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 8, 2012
- [FDA Inspection 638785 - Sunny Delight Beverages Company - 2010-01-12](https://www.keypedia.com/records/fda_inspections/sunny-delight-beverages-company/8ea4ccea-d791-4131-a336-23c1d93664f4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 12, 2010

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