# HertART ApS – FDA Inspection, Mar 21, 2018

Source: https://www.keypedia.com/records/fda_inspections/hertart-aps/9e1c533f-5d1f-4633-b7cc-99be7af74fc8
Source feed: FDA_Inspections

> FDA inspection 1047589 of HertART ApS, March 21, 2018. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 803 and 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1047589
- Company Name: HertART ApS
- Inspection Date: 2018-03-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 1220574 - 2023-08-28
- FDA Inspection 927679 - 2015-04-29

## Related Officers

- [Investigator](https://www.keypedia.com/people/catherine-j-laufmann/920b7656-2847-408d-ba15-3989283d8c94)

Company: https://www.keypedia.com/companies/hertart-aps/a8996873-2ce8-4b77-8863-d47f3b795828

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