# R2 Diagnostics, Inc. – FDA Inspection, Jan 31, 2018

Source: https://www.keypedia.com/records/fda_inspections/r2-diagnostics-inc/6b6bad9a-85ac-4da9-b299-18326ae10f8d
Source feed: FDA_Inspections

> FDA inspection 1040085 of R2 Diagnostics, Inc., January 31, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040085
- Company Name: R2 Diagnostics, Inc.
- Inspection Date: 2018-01-31
- 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: 2

## Related Documents

- FDA Inspection 1159391 - 2021-12-09
- [FDA Inspection 936833 - 2015-08-04](https://www.keypedia.com/records/fda_inspections/r2-diagnostics-inc/1caab37b-2564-43d6-bb64-63d53795fa5e)

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/suyang-qin/c32419c5-1b78-4014-9f94-cb7ab17dfe05)

Company: https://www.keypedia.com/companies/r2-diagnostics-inc/b89a8ca1-755b-4e71-afc5-b03026a97d4a

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