# Royal Cup, Inc - Inspection Records

Source: https://www.keypedia.com/companies/royal-cup-inc/4aa8e35f-1c8a-4470-92d7-0a2d8db5d015

> Inspection records and compliance data for Royal Cup, Inc in Mobile, Alabama. Access full analysis and detailed observations.

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## Details

- Name: Royal Cup, Inc
- FEI Number: 3004339402
- City: Mobile
- State: Alabama
- Country Name: United States
- Address Line 1: 1900 S Broad St Ste A
- Zip Code: 36615

## Related Documents

- [FDA Inspection 1307076 - Royal Cup, Inc - 2026-02-19](https://www.keypedia.com/records/fda_inspections/royal-cup-inc/c2fbf72c-d742-400b-ba22-7764ac6510b2) — source: FDA, date: February 19, 2026
- [FDA Inspection 1307076 - Royal Cup, Inc - 2026-02-19](https://www.keypedia.com/records/fda_inspections/royal-cup-inc/90539ab9-1290-4618-8b3c-bd856f63480e) — classification: No Action Indicated (NAI), source: FDA, date: February 19, 2026
- [FDA Inspection 1178727 - Royal Cup, Inc - 2022-06-22](https://www.keypedia.com/records/fda_inspections/royal-cup-inc/c54d3d74-53fe-4b6f-b6cc-705c1844c3b1) — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2022
- [FDA Inspection 1022731 - Royal Cup, Inc - 2017-08-09](https://www.keypedia.com/records/fda_inspections/royal-cup-inc/ef619abb-a60e-4a83-adf7-fc84280cf4a7) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 9, 2017
- [FDA Inspection 1022731 - Royal Cup, Inc - 2017-08-09](https://www.keypedia.com/records/fda_inspections/royal-cup-inc/cb1a719f-f4e3-42bd-8d9b-c37f3030c28d) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 9, 2017
- [FDA Inspection 1022731 - Royal Cup, Inc - 2017-08-09](https://www.keypedia.com/records/fda_inspections/royal-cup-inc/3c38ee8e-2d3b-4b90-b1c8-42a55fea3383) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 9, 2017
- [FDA Inspection 985151 - Royal Cup, Inc - 2016-09-13](https://www.keypedia.com/records/fda_inspections/royal-cup-inc/06211fcd-51cb-48a8-8776-8e4162904f09) — classification: Voluntary Action Indicated (VAI), source: FDA, date: September 13, 2016

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