# Sugar Daddy  LTD, Saint Louis, MO – FDA Inspections

Source: https://www.keypedia.com/companies/sugar-daddy-ltd/6c20b5fa-7be7-4356-9cab-9741e115d592

> Inspection records and compliance data for Sugar Daddy  LTD in Saint Louis, Missouri. 6 FDA inspections on record (1 OAI), 3 Form 483s, last inspected May 23, 2025.

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## Details

- Name: Sugar Daddy  LTD
- FEI Number: 1940680
- Address Line 1: 4000 S Grand Blvd
- City: Saint Louis
- State: Missouri
- Zip Code: 63118
- Country Name: United States
- Address: 4000 S Grand Blvd, Saint Louis, Missouri 63118, United States
- Country: United States

## Related Documents

- FDA Inspection 1270979 - Sugar Daddy  LTD - 2025-05-23 — source: FDA, date: May 23, 2025
- [FDA Inspection 1208438 - Sugar Daddy  LTD - 2023-06-09](https://www.keypedia.com/records/fda_inspections/sugar-daddy-ltd/4b852f3f-a342-4f86-9662-1ea6b1312acf) — source: FDA, date: June 9, 2023
- [FDA Inspection 1100082 - Sugar Daddy  LTD - 2019-08-15](https://www.keypedia.com/records/fda_inspections/sugar-daddy-ltd/f7d2df37-aa50-4657-8b32-899e5d9920d8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 15, 2019
- FDA Inspection 1100082 - Sugar Daddy  LTD - 2019-08-15 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 15, 2019
- [FDA Inspection 1068505 - Sugar Daddy  LTD - 2018-10-12](https://www.keypedia.com/records/fda_inspections/sugar-daddy-ltd/d948df9f-8df7-4488-a890-a5c775d604c0) — classification: Official Action Indicated (OAI), source: FDA, date: October 12, 2018
- FDA Inspection 1068505 - Sugar Daddy  LTD - 2018-10-12 — classification: Official Action Indicated (OAI), source: FDA, date: October 12, 2018
- [FDA Inspection 949226 - Sugar Daddy  LTD - 2015-10-23](https://www.keypedia.com/records/fda_inspections/sugar-daddy-ltd/22a25caf-e480-429d-9495-40451747578f) — classification: Voluntary Action Indicated (VAI), source: FDA, date: October 23, 2015
- FDA Inspection 909181 - Sugar Daddy  LTD - 2014-12-22 — classification: No Action Indicated (NAI), source: FDA, date: December 22, 2014

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