# FDA Inspection 571672 - Trimline Medical Products Corp - March 24, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/trimline-medical-products-corp/cca91623-0c21-40e9-a963-7fe8e96a7325
Source feed: FDA_Inspections

> FDA Inspection 571672 for Trimline Medical Products Corp on March 24, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 571672
- Company Name: Trimline Medical Products Corp
- Inspection Date: 2009-03-24
- 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 571672 - 2009-03-24](https://www.globalkeysolutions.net/records/fda_inspections/trimline-medical-products-corp/dea49ff9-37c4-4354-af01-49b5a92badc0)

Company: https://www.globalkeysolutions.net/companies/trimline-medical-products-corp/2384f9f5-4871-464e-87ab-1952ec627f10

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