# FDA Inspection 728886 - Lasertel, Inc. - May 26, 2011

Source: https://www.keypedia.com/records/fda_inspections/lasertel-inc/7cdae5d6-af53-4fce-a581-f9990bd4da4b
Source feed: FDA_Inspections

> FDA Inspection 728886 for Lasertel, Inc. on May 26, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 728886
- Company Name: Lasertel, Inc.
- Inspection Date: 2011-05-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 884757 - 2014-06-19](https://www.keypedia.com/records/fda_inspections/lasertel-inc/974eb27d-02ce-408a-87c9-f82f70a5ddfd)

Company: https://www.keypedia.com/companies/lasertel-inc/0f1ae2fe-5471-42d7-b088-f0fd06480b47

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