# FDA Inspection 1258485 - Atmos Medizintechnik Gmbh & Co. KG - January 16, 2025

Source: https://www.keypedia.com/records/fda_inspections/atmos-medizintechnik-gmbh-co-kg/39d05071-dd7d-4bad-bfa5-53a0caf0f1c0
Source feed: FDA_Inspections

> FDA Inspection 1258485 for Atmos Medizintechnik Gmbh & Co. KG on January 16, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1258485
- Company Name: Atmos Medizintechnik Gmbh & Co. KG
- Inspection Date: 2025-01-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1258485 - 2025-01-16](https://www.keypedia.com/records/fda_inspections/atmos-medizintechnik-gmbh-co-kg/ef80b5f9-ffec-4916-ac21-c4bea15cb60b)
- [FDA Inspection 1258485 - 2025-01-16](https://www.keypedia.com/records/fda_inspections/atmos-medizintechnik-gmbh-co-kg/f4416285-717d-4276-b25e-60054718ba88)

Company: https://www.keypedia.com/companies/atmos-medizintechnik-gmbh-co-kg/25474050-d561-44d0-a912-5f261343d2b6

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