# Muhanna Sweets (USA), Inc, Tulsa, OK – FDA Inspections

Source: https://www.keypedia.com/companies/muhanna-sweets-usa-inc/e4b22d54-f49b-4970-8682-49c6c9f6cdd0

> Inspection records and compliance data for Muhanna Sweets (USA), Inc in Tulsa, Oklahoma. 6 FDA inspections on record, last inspected January 28, 2025.

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## Details

- Name: Muhanna Sweets (USA), Inc
- FEI Number: 3004685201
- Address Line 1: 6104 E 71st St Ste 22
- City: Tulsa
- State: Oklahoma
- Zip Code: 74136
- Country Name: United States
- Address: 6104 E 71st St Ste 22, Tulsa, Oklahoma 74136, United States
- Country: United States

## Related Documents

- FDA Inspection 1260640 - Muhanna Sweets (USA), Inc - 2025-01-28 — source: FDA, date: January 28, 2025
- FDA Inspection 1260640 - Muhanna Sweets (USA), Inc - 2025-01-28 — classification: No Action Indicated (NAI), source: FDA, date: January 28, 2025
- FDA Inspection 1174778 - Muhanna Sweets (USA), Inc - 2022-07-12 — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2022
- FDA Inspection 1174778 - Muhanna Sweets (USA), Inc - 2022-07-12 — classification: No Action Indicated (NAI), source: FDA, date: July 12, 2022
- FDA Inspection 1036945 - Muhanna Sweets (USA), Inc - 2017-11-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: November 29, 2017
- FDA Inspection 900437 - Muhanna Sweets (USA), Inc - 2014-10-21 — classification: No Action Indicated (NAI), source: FDA, date: October 21, 2014
- [FDA Inspection 821653 - Muhanna Sweets (USA), Inc - 2013-01-29](https://www.keypedia.com/records/fda_inspections/muhanna-sweets-usa-inc/73f98e40-4e69-487b-ba88-4d51601d4851) — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2013
- FDA Inspection 727195 - Muhanna Sweets (USA), Inc - 2011-05-05 — classification: No Action Indicated (NAI), source: FDA, date: May 5, 2011
- FDA Inspection 727195 - Muhanna Sweets (USA), Inc - 2011-05-05 — classification: No Action Indicated (NAI), source: FDA, date: May 5, 2011
- FDA Inspection 727195 - Muhanna Sweets (USA), Inc - 2011-05-05 — classification: No Action Indicated (NAI), source: FDA, date: May 5, 2011

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