# Aktina Medical Corp – FDA Inspection, Jul 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/aktina-medical-corp/4cfefa03-84e4-45e3-a6e4-b1141a55cac7
Source feed: FDA_Inspections

> FDA inspection 1018921 of Aktina Medical Corp, July 24, 2017. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1018921
- Company Name: Aktina Medical Corp
- Inspection Date: 2017-07-24
- 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: 3

## Related Documents

- FDA Inspection 818494 - 2013-02-12
- FDA Inspection 629447 - 2009-11-06

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gregson-a-joseph/90bf8118-3f32-4f44-95c4-fcde1f741a18)

Company: https://www.keypedia.com/companies/aktina-medical-corp/d78d799a-6e65-4b26-825a-766d98946ebb

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