# FDA Inspection 1010961 - Peter Kosek - April 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/peter-kosek/14cedfb9-1119-404b-878c-7006f37bbf6b
Source feed: FDA_Inspections

> FDA Inspection 1010961 for Peter Kosek on April 21, 2017. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1010961
- Company Name: Peter Kosek
- Inspection Date: 2017-04-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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