# FDA Inspection 909561 - Ante Laser Technology Co. Ltd. - November 07, 2014

Source: https://www.keypedia.com/records/fda_inspections/ante-laser-technology-co-ltd/d6a42fa1-d41b-48d4-964d-0d8337b37d74
Source feed: FDA_Inspections

> FDA Inspection 909561 for Ante Laser Technology Co. Ltd. on November 07, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 909561
- Company Name: Ante Laser Technology Co. Ltd.
- Inspection Date: 2014-11-07
- Classification: Voluntary Action Indicated (VAI)
- 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/ante-laser-technology-co-ltd/15fdde72-cc5d-431c-a644-49da934df69f

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