# FDA Inspection 911856 - Precision X-ray, Inc. - January 26, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/precision-x-ray-inc/ef9f608d-20aa-4110-9b41-6a490d373d0e
Source feed: FDA_Inspections

> FDA Inspection 911856 for Precision X-ray, Inc. on January 26, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 911856
- Company Name: Precision X-ray, Inc.
- Inspection Date: 2015-01-26
- 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 758996 - 2011-12-15](https://www.globalkeysolutions.net/records/fda_inspections/precision-x-ray-inc/ff32e4c1-1079-4809-accf-aa12f8ee929f)

Company: https://www.globalkeysolutions.net/companies/precision-x-ray-inc/9aa11dc6-8f82-4023-99b3-e7f7f8ecace2

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