# Kinamed Inc – FDA Inspection, Aug 27, 2026

Source: https://www.keypedia.com/records/fda_inspections/kinamed-inc/dccd1e54-3824-4675-bd89-fe671aeeb8d2
Source feed: FDA_Inspections

> FDA inspection 1333118 of Kinamed Inc, August 27, 2026. Classification: Voluntary Action Indicated (VAI). 1 citation. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1333118
- Company Name: Kinamed Inc
- Inspection Date: 2026-08-27
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Los Angeles District Office
- Citation Count: 1

## Related Documents

- FDA Inspection 1117751 - 2020-02-12
- FDA Inspection 980471 - 2016-07-21
- FDA Inspection 875744 - 2014-04-14
- FDA Inspection 773213 - 2012-03-15
- [FDA Inspection 663654 - 2010-06-01](https://www.keypedia.com/records/fda_inspections/kinamed-inc/97761693-6e24-48ef-84dd-fcef723b9e20)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sarah-a-hassas/4f142d54-fc28-4bd5-82ad-7e6fa443688c)

Company: https://www.keypedia.com/companies/kinamed-inc/952c9674-441f-43ae-887a-5d9124290519

Office: https://www.keypedia.com/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b