# Peter Kosek – FDA Inspection, Apr 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/peter-kosek/456046f8-6f18-4f10-a0d1-f8612def9f30
Source feed: FDA_Inspections

> FDA inspection 1010961 of Peter Kosek, April 21, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 50. Form 483 issued.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1010961
- Company Name: Peter Kosek
- Inspection Date: 2017-04-21
- 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: 3

## Related Officers

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

Company: https://www.keypedia.com/companies/peter-kosek/46ce69dd-fc7b-4359-b2b8-b70349bf7a86

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