# Hocoma AG – FDA Inspection, Jul 11, 2024

Source: https://www.keypedia.com/records/fda_inspections/hocoma-ag/c2db049d-c038-4a27-a0b3-2352ccdd8bad
Source feed: FDA_Inspections

> FDA inspection 1245475 of Hocoma AG, July 11, 2024. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1245475
- Company Name: Hocoma AG
- Inspection Date: 2024-07-11
- 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: 1

## Related Documents

- FDA Inspection 1036878 - 2017-12-07

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/daniel-j-lahar/d4e329c0-b6a5-42ca-acde-b79413b245ea)

Company: https://www.keypedia.com/companies/hocoma-ag/12b4fe5b-fddc-4ffb-a136-cfd358e40531

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