# Avalign Delivery Systems Division – FDA Inspection, May 23, 2018

Source: https://www.keypedia.com/records/fda_inspections/avalign-delivery-systems-division/ee9ceb13-8351-416c-a121-fe9a8c965200
Source feed: FDA_Inspections

> FDA inspection 1053732 of Avalign Delivery Systems Division, May 23, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1053732
- Company Name: Avalign Delivery Systems Division
- Inspection Date: 2018-05-23
- 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: 2

## Related Documents

- [FDA Inspection 889789 - 2014-08-05](https://www.keypedia.com/records/fda_inspections/avalign-delivery-systems-division/e2bdeb48-cb53-45c0-9657-1d357d3ccc34)
- FDA Inspection 793541 - 2012-08-09
- FDA Inspection 580993 - 2009-04-30

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/joseph-r-strelnik/1fb7d50e-abf2-45ef-85a8-71c61b33e42d)

Company: https://www.keypedia.com/companies/avalign-delivery-systems-division/654c7764-0843-46a9-b9cc-6f27d6a8606c

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