# Cersys, Inc – FDA Inspection, Aug 23, 2013

Source: https://www.keypedia.com/records/fda_inspections/cersys-inc/ed0e3319-08ef-468e-a5f0-1544e51bdecd
Source feed: FDA_Inspections

> FDA inspection 846710 of Cersys, Inc, August 23, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 846710
- Company Name: Cersys, Inc
- Inspection Date: 2013-08-23
- 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: 4

Company: https://www.keypedia.com/companies/cersys-inc/f8c87d1d-15f2-4703-8ce4-801fbdcc85a3

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