# FDA Inspection 586850 - Transverse Industries Co., Ltd. - April 08, 2009

Source: https://www.keypedia.com/records/fda_inspections/transverse-industries-co-ltd/3dac354a-80ac-471d-a78b-3ed36bc73967
Source feed: FDA_Inspections

> FDA Inspection 586850 for Transverse Industries Co., Ltd. on April 08, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 586850
- Company Name: Transverse Industries Co., Ltd.
- Inspection Date: 2009-04-08
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/transverse-industries-co-ltd/37dc622e-f35a-47b6-a305-835c04519d89

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