# Wolf X-Ray Corp – FDA Inspection, May 8, 2018

Source: https://www.keypedia.com/records/fda_inspections/wolf-x-ray-corp/5d0b21f1-b6a5-4167-9317-0e972f9db0e5
Source feed: FDA_Inspections

> FDA inspection 1051321 of Wolf X-Ray Corp, May 08, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051321
- Company Name: Wolf X-Ray Corp
- Inspection Date: 2018-05-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

- FDA Inspection 1046334 - 2018-03-14
- [FDA Inspection 933484 - 2015-07-07](https://www.keypedia.com/records/fda_inspections/wolf-x-ray-corp/b4187491-62b2-4bad-a849-f479f4eb5ea6)
- FDA Inspection 820732 - 2013-03-01
- FDA Inspection 731640 - 2011-06-24
- FDA Inspection 731630 - 2011-06-24

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/andrew-j-garufi/567f6aaa-f6f2-45a3-9a58-80b33f3ad021)

Company: https://www.keypedia.com/companies/wolf-x-ray-corp/adf37c72-f3e6-4f4e-82c9-9e5c79c59710

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