# LINA Medical Aps – FDA Inspection, Nov 1, 2017

Source: https://www.keypedia.com/records/fda_inspections/lina-medical-aps/ca68ae14-0165-499d-a769-437387a583cd
Source feed: FDA_Inspections

> FDA inspection 1031380 of LINA Medical Aps, November 01, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031380
- Company Name: LINA Medical Aps
- Inspection Date: 2017-11-01
- 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 719043 - 2011-03-22](https://www.keypedia.com/records/fda_inspections/lina-medical-aps/f6b6fdac-4cbc-4a4e-9a3a-00424ab1022f)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/lina-medical-aps/11335b35-dbc4-42fa-a051-8710f6b4de24

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