# Ronald F. Budzik Jr., MD – FDA Inspection, Oct 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/ronald-f-budzik-jr-md/62b1da68-6ca8-442d-9b92-8807317dfeec
Source feed: FDA_Inspections

> FDA inspection 1028855 of Ronald F. Budzik Jr., MD, October 17, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028855
- Company Name: Ronald F. Budzik Jr., MD
- Inspection Date: 2017-10-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Project Evaluation: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- FDA Inspection 1118258 - 2020-01-16

## Related Officers

- [Company Rep](https://www.keypedia.com/people/geoffrey-k-kilili/b00aeedf-95bd-4ccf-a23e-6e12e60249c4)

Company: https://www.keypedia.com/companies/ronald-f-budzik-jr-md/35cbe754-5aa2-4042-a402-bd05aeee20b0

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