# Dyna-Tek Industries – FDA Inspection, Jan 24, 2013

Source: https://www.keypedia.com/records/fda_inspections/dyna-tek-industries/2da1ab8a-59cd-48b8-82b5-1d98568c173e
Source feed: FDA_Inspections

> FDA inspection 817627 of Dyna-Tek Industries, January 24, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 817627
- Company Name: Dyna-Tek Industries
- Inspection Date: 2013-01-24
- 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 636306 - 2010-01-06

Company: https://www.keypedia.com/companies/dyna-tek-industries/9b1d38ee-8e44-4cee-9706-826a10aeda6a

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