# FDA Inspection 1283240 - Myron L Company - September 19, 2025

Source: https://www.keypedia.com/records/fda_inspections/myron-l-company/e26d6328-2f35-4012-9163-a9cd555c19bc
Source feed: FDA_Inspections

> FDA Inspection 1283240 for Myron L Company on September 19, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1283240
- Company Name: Myron L Company
- Inspection Date: 2025-09-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/myron-l-company/5ebef52d-5c22-42e2-a337-a79e56fc5b89

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7
