# FDA Inspection 1265539 - Medi-Dyne Healthcare Products, Ltd - March 26, 2025

Source: https://www.keypedia.com/records/fda_inspections/medi-dyne-healthcare-products-ltd/33727722-9579-4f5a-8d47-71fea46efe8a
Source feed: FDA_Inspections

> FDA Inspection 1265539 for Medi-Dyne Healthcare Products, Ltd on March 26, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1265539
- Company Name: Medi-Dyne Healthcare Products, Ltd
- Inspection Date: 2025-03-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1265539 - 2025-03-26](https://www.keypedia.com/records/fda_inspections/medi-dyne-healthcare-products-ltd/3053188f-5a12-4dbf-8fa3-b674cd47fd2a)
- [FDA Inspection 1265539 - 2025-03-26](https://www.keypedia.com/records/fda_inspections/medi-dyne-healthcare-products-ltd/7b7bf58d-c268-4131-905b-cc7f93a1720e)

Company: https://www.keypedia.com/companies/medi-dyne-healthcare-products-ltd/4bf10211-23c6-4481-a3b3-7dbdfe61e169

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