# Homtex Inc – FDA Inspection, Oct 16, 2025

Source: https://www.keypedia.com/records/fda_inspections/homtex-inc/9935b846-3e67-4251-9eba-57d90e752ff0
Source feed: FDA_Inspections

> FDA inspection 1288366 of Homtex Inc, October 16, 2025. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1288366
- Company Name: Homtex Inc
- Inspection Date: 2025-10-16
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: New Orleans District Office
- Citation Count: 2

## Related Officers

- [Company Rep](https://www.keypedia.com/people/nikki-s-bryant/fe859d4f-23a6-4bc9-94c6-5b3c3fe8d99a)

Company: https://www.keypedia.com/companies/homtex-inc/ba2e0ff4-48b0-4c32-bfac-e105288cd746

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