# Zyga Technology, Inc. – FDA Inspection, Oct 3, 2012

Source: https://www.keypedia.com/records/fda_inspections/zyga-technology-inc/29b38cba-d897-42a0-a3c5-135038d3fe27
Source feed: FDA_Inspections

> FDA inspection 803692 of Zyga Technology, Inc., October 03, 2012. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 803692
- Company Name: Zyga Technology, Inc.
- Inspection Date: 2012-10-03
- 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

## Related Documents

- FDA Inspection 1040488 - 2018-02-07
- FDA Inspection 937015 - 2015-07-22

Company: https://www.keypedia.com/companies/zyga-technology-inc/b4aeb66e-9cb6-4210-ad27-c871adf25c36

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