# Rejoni, Inc. – FDA Inspection, Jul 9, 2025

Source: https://www.keypedia.com/records/fda_inspections/rejoni-inc/7794bdb2-3d74-4206-b877-69bfddc671cd
Source feed: FDA_Inspections

> FDA inspection 1275287 of Rejoni, Inc., July 09, 2025. Classification: Official Action Indicated (OAI). 1 citation under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1275287
- Company Name: Rejoni, Inc.
- Inspection Date: 2025-07-09
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Product Evaluation: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New England District Office
- Citation Count: 1

## Related Documents

- FDA Inspection 1302726 - 2026-02-09

## Related Officers

- [Meredith L. Miller](https://www.keypedia.com/people/meredith-l-miller/c775003b-4e5b-48d8-bc51-1a3ebe813dba)

Company: https://www.keypedia.com/companies/rejoni-inc/5dfbfff9-b468-4479-b150-e9bcd65e8116

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144