# Encompass Group LLC – FDA 483, Jul 2, 2026

Source: https://www.keypedia.com/records/483/encompass-group-llc/7bd71999-c502-4c04-934c-48664ba0d60d

> FDA 483 for Encompass Group LLC on July 02, 2026. Product: device. Access full analysis and detailed observations.

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## Details

- Record Type: 483
- Company Name: Encompass Group LLC
- Inspection Date: 2026-07-02
- Product Type: device
- Office Name: Atlanta District Office
- Summary: Encompass Group LLC, a medical device manufacturer in McDonough, GA, was inspected and received a Form 483 with three observations. The inspection revealed significant deficiencies in the firm's quality management system, including inadequate corrective and preventive actions, a lack of timely internal audits, and insufficient maintenance of personnel training records. Several issues, particularly regarding internal audits and training, were repeats from previous inspections, indicating persistent non-compliance.

## Related Documents

- [EIR - 2020-01-08](https://www.keypedia.com/records/eir/encompass-group-llc/c583bf94-34e1-41a6-8e7b-96ad349b2970) — date: January 8, 2020

## Related Officers

- [Dawn M. Braswell](https://www.keypedia.com/people/dawn-m-braswell/6a66fdbb-fff8-4b4b-9f06-320464957b87)

Company: https://www.keypedia.com/companies/encompass-group-llc/f5e995b2-49c4-482d-9c23-9254222e32db

Office: https://www.keypedia.com/offices/atlanta-district-office/7586d99a-288e-49d1-8c3d-d88b7354b7a7