# FDA Inspection 927679 - HertART ApS - April 29, 2015

Source: https://www.keypedia.com/records/fda_inspections/hertart-aps/202e147b-80f7-4235-b124-4cdffb7c17e9
Source feed: FDA_Inspections

> FDA Inspection 927679 for HertART ApS on April 29, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 927679
- Company Name: HertART ApS
- Inspection Date: 2015-04-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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