# FDA Inspection 1071189 - WEBER MEDICAL GMBH - November 08, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/weber-medical-gmbh/9e51c108-6328-4884-a819-5c97963b1a0e
Source feed: FDA_Inspections

> FDA Inspection 1071189 for WEBER MEDICAL GMBH on November 08, 2018. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1071189
- Company Name: WEBER MEDICAL GMBH
- Inspection Date: 2018-11-08
- Classification: Official Action Indicated (OAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1190292 - 2022-09-22](https://www.globalkeysolutions.net/records/fda_inspections/weber-medical-gmbh/a05ea4c3-620d-47e7-8e10-b4adac886163)
- [FDA Inspection 1190292 - 2022-09-22](https://www.globalkeysolutions.net/records/fda_inspections/weber-medical-gmbh/c39d0a39-253d-4a08-81b6-90daf75620ac)
- [FDA Inspection 1071189 - 2018-11-08](https://www.globalkeysolutions.net/records/fda_inspections/weber-medical-gmbh/ec8c7241-86bf-49c1-a7d2-0502510d7ff2)
- [FDA Inspection 817804 - 2013-01-17](https://www.globalkeysolutions.net/records/fda_inspections/weber-medical-gmbh/10e422e8-3bc0-42ed-823b-d45f2fdda26b)

Company: https://www.globalkeysolutions.net/companies/weber-medical-gmbh/750376b8-e96f-41fc-a95f-21bfa440787e

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