# Asteelflash Design Solutions Hamburg GmbH – FDA Inspection, May 9, 2019

Source: https://www.keypedia.com/records/fda_inspections/asteelflash-design-solutions-hamburg-gmbh/cb20766f-b513-43cf-a9c3-ff8739df7d29
Source feed: FDA_Inspections

> FDA inspection 1090087 of Asteelflash Design Solutions Hamburg GmbH, May 09, 2019. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1090087
- Company Name: Asteelflash Design Solutions Hamburg GmbH
- Inspection Date: 2019-05-09
- 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: 5

## Related Officers

- [Investigator](https://www.keypedia.com/people/stephen-r-souza/9b7af4df-f1cc-468d-9761-cee11d3c14fc)

Company: https://www.keypedia.com/companies/asteelflash-design-solutions-hamburg-gmbh/ec81d0ac-6595-4ed4-81c0-872c5ab5d7f4

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