# WCG IRB, Inc – FDA Inspection, Aug 24, 2018

Source: https://www.keypedia.com/records/fda_inspections/wcg-irb-inc/d9e5bc35-a688-42f3-a6a8-2a22f61e3582
Source feed: FDA_Inspections

> FDA inspection 1063861 of WCG IRB, Inc, August 24, 2018. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 50. Form 483 issued. 7 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1063861
- Company Name: WCG IRB, Inc
- Inspection Date: 2018-08-24
- 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: 1

## Related Documents

- FDA Inspection 1156516 - 2021-11-05
- [FDA Inspection 908369 - 2014-11-12](https://www.keypedia.com/records/fda_inspections/wcg-irb-inc/13597f80-a9fe-4616-be7e-089cec4e1ba1)
- FDA Inspection 818286 - 2013-02-14
- [FDA Inspection 754491 - 2011-11-09](https://www.keypedia.com/records/fda_inspections/wcg-irb-inc/835b92fd-6bdf-49b0-8c69-e4d58dd6de2e)
- FDA Inspection 723222 - 2011-05-11

## Related Officers

- [Company Rep](https://www.keypedia.com/people/sherri-n-rohlf/41090ab1-83d1-4e95-92ea-0cfca5cecdb6)

Company: https://www.keypedia.com/companies/wcg-irb-inc/f755e1b3-f395-409e-99c5-4374ae81366f

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