# FDA Inspection 638097 - Telesis Technologies, Inc. - December 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/telesis-technologies-inc/c565bbc2-c2ea-4ac8-8498-1cb4ad8c54c3
Source feed: FDA_Inspections

> FDA Inspection 638097 for Telesis Technologies, Inc. on December 09, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 638097
- Company Name: Telesis Technologies, Inc.
- Inspection Date: 2009-12-09
- 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/telesis-technologies-inc/71b8d4f2-20ca-478a-bc3b-36f82f019d17

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