# FDA 483 - MPP GROUP, LLC - September 11, 2018

Source: https://www.keypedia.com/records/483/mpp-group-llc/0c7e4645-0030-402e-a0e0-ae9f87edcc6b

> FDA 483 for MPP GROUP, LLC on September 11, 2018. Product: other. Access full analysis and detailed observations.

---

## Details

- Record Type: 483
- Company Name: MPP GROUP, LLC
- Inspection Date: 2018-09-11
- Product Type: other
- Office Name: Minneapolis District Office
- Summary: MEP GROUP, LLC, a dietary supplement manufacturer in Mequon, WI, was cited for multiple quality control deficiencies during an FDA inspection. The firm failed to perform identity testing on dietary ingredients, improperly approved components, and did not adequately qualify suppliers. Additionally, the company distributed finished batches without quality release and failed to maintain readily available master manufacturing records.

## Related Documents

- [483 - Unknown Date](https://www.keypedia.com/records/483/mpp-group-llc/8003783e-448c-48bb-9865-37d60b3b73b9)

## Related Officers

- [Alecia Marson](https://www.keypedia.com/people/alecia-marson/be80cbdb-e914-4e6a-ab47-44eb0adbf04e)

Company: https://www.keypedia.com/companies/mpp-group-llc/055da328-30b8-49d7-975f-4caf69d4de2b

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d