# FDA 483 - MRP, LLC dba Aquabiliti - October 18, 2022

Source: https://www.keypedia.com/records/483/mrp-llc-dba-aquabiliti/c990fd1d-4c46-4e4f-9044-05609656a633

> FDA 483 for MRP, LLC dba Aquabiliti on October 18, 2022. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: MRP, LLC dba Aquabiliti
- Inspection Date: 2022-10-18
- Product Type: device
- Office Name: New Orleans District Office
- Summary: MRP, LLC dba Aquabiliti in Nashville, TN, was inspected and received a Form 483 with two observations. The inspection revealed inadequate procedures for controlling storage areas, leading to product mix-up risks and issues with material identification. Additionally, the firm failed to adequately document corrective and preventive actions related to Design History File updates for their sterile flush syringes.

## Related Documents

- [483 - 2020-02-27](https://www.keypedia.com/records/483/mrp-llc-dba-aquabiliti/90574e3f-9c8d-466b-9a91-8762d630cba5)

## Related Officers

- [Jamie P. Webb](https://www.keypedia.com/people/jamie-p-webb/9e052469-54f7-4d56-b977-27babbdac09b)
- [Mary A. Millner](https://www.keypedia.com/people/mary-a-millner/bd8911cf-849d-41d2-ae12-dd4bad66e798)

Company: https://www.keypedia.com/companies/mrp-llc-dba-aquabiliti/f96d032d-ca2d-4610-ad28-28231b305167

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