# Heidelberg Medical Inc – FDA Inspection, Feb 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/heidelberg-medical-inc/5d4f3b7b-84f6-4fc8-805e-3fe453d6de64
Source feed: FDA_Inspections

> FDA inspection 1012625 of Heidelberg Medical Inc, February 24, 2017. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1012625
- Company Name: Heidelberg Medical Inc
- Inspection Date: 2017-02-24
- 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 Officers

- [Company Rep](https://www.keypedia.com/people/ana-l-kewes/6b1c7d79-5cea-4939-aebd-0f67f53cb879)

Company: https://www.keypedia.com/companies/heidelberg-medical-inc/36fb69bc-468e-4fc6-a527-1decd6a4663c

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