# The American Bottling Company dba Seven Up Snapple Southeast, Orlando, FL – FDA Inspections

Source: https://www.keypedia.com/companies/the-american-bottling-company-dba-seven-up-snapple-southeast/93d3927a-53a6-4168-9681-d696727c919a

> Inspection records and compliance data for The American Bottling Company dba Seven Up Snapple Southeast in Orlando, Florida. 3 FDA inspections on record, last inspected March 23, 2026.

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## Details

- Name: The American Bottling Company dba Seven Up Snapple Southeast
- FEI Number: 3004337758
- Address Line 1: 1181 Tradeport Dr
- City: Orlando
- State: Florida
- Zip Code: 32824
- Country Name: United States
- Address: 1181 Tradeport Dr, Orlando, Florida 32824, United States
- Country: United States

## Related Documents

- [FDA Inspection 1310692 - The American Bottling Company dba Seven Up Snapple Southeast - 2026-03-23](https://www.keypedia.com/records/fda_inspections/the-american-bottling-company-dba-seven-up-snapple-southeast/73faf0e8-b3f6-4f85-b33d-9b966219d406) — source: FDA, date: March 23, 2026
- FDA Inspection 1310692 - The American Bottling Company dba Seven Up Snapple Southeast - 2026-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2026
- FDA Inspection 1310692 - The American Bottling Company dba Seven Up Snapple Southeast - 2026-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2026
- FDA Inspection 1072889 - The American Bottling Company dba Seven Up Snapple Southeast - 2018-10-10 — classification: No Action Indicated (NAI), source: FDA, date: October 10, 2018
- FDA Inspection 1072889 - The American Bottling Company dba Seven Up Snapple Southeast - 2018-10-10 — classification: No Action Indicated (NAI), source: FDA, date: October 10, 2018
- FDA Inspection 763447 - The American Bottling Company dba Seven Up Snapple Southeast - 2012-01-06 — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 6, 2012
- FDA Inspection 763447 - The American Bottling Company dba Seven Up Snapple Southeast - 2012-01-06 — classification: No Action Indicated (NAI), source: FDA, date: January 6, 2012

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