# FDA 483 - Potty MD LLC - February 18, 2022

Source: https://www.keypedia.com/records/483/potty-md-llc/41230f1c-48b7-4a5c-acb3-f2d02252dae1

> FDA 483 for Potty MD LLC on February 18, 2022. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Potty MD LLC
- Inspection Date: 2022-02-18
- Product Type: device
- Office Name: New Orleans District Office
- Summary: An FDA inspection of Potty MD LLC in Knoxville, TN, a specification developer, revealed two significant observations. The firm failed to adequately maintain complaint files by not documenting oral complaints and did not properly maintain device history records for acceptance activities and testing of the Wet-Stop 3+ device.

## Related Officers

- [Benjamin E. Bowen](https://www.keypedia.com/people/benjamin-e-bowen/7fdc5755-0d5d-45c9-93a0-3cb928156c1d)

Company: https://www.keypedia.com/companies/potty-md-llc/62022b87-686e-4d5d-83de-ed1147ef299b

Office: https://www.keypedia.com/offices/new-orleans-district-office/95352142-b992-4e06-849d-d7483c0959ea