# FDA Inspection 593495 - Lasercraft, Inc. - June 24, 2009

Source: https://www.keypedia.com/records/fda_inspections/lasercraft-inc/1c05521e-3ef1-436d-866b-b885a95df00a
Source feed: FDA_Inspections

> FDA Inspection 593495 for Lasercraft, Inc. on June 24, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 593495
- Company Name: Lasercraft, Inc.
- Inspection Date: 2009-06-24
- 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/lasercraft-inc/2ecaf859-7143-4d87-8754-a62cece97680

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