# FDA Inspection 1051603 - Angiomed GmbH & Co. Medizintechnik KG - April 12, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/angiomed-gmbh-co-medizintechnik-kg/fa5eeb6a-7ce0-4f71-bf5e-a011088f4182/
Source feed: FDA_Inspections

> FDA Inspection 1051603 for Angiomed GmbH & Co. Medizintechnik KG on April 12, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051603
- Company Name: Angiomed GmbH & Co. Medizintechnik KG
- Inspection Date: 2018-04-12
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1051603 - 2018-04-12](https://www.globalkeysolutions.net/api/records/fda_inspections/angiomed-gmbh-co-medizintechnik-kg/730eb3a8-52de-4f19-9ba0-e3e9889d9267/)
- [FDA Inspection 953098 - 2015-08-20](https://www.globalkeysolutions.net/api/records/fda_inspections/angiomed-gmbh-co-medizintechnik-kg/8c9cdfdb-e36c-46bd-8bf8-1fa8eb4239bd/)
- [FDA Inspection 812973 - 2012-12-13](https://www.globalkeysolutions.net/api/records/fda_inspections/angiomed-gmbh-co-medizintechnik-kg/0c83f1c9-377e-4669-bc21-dcaf517c3152/)
- [FDA Inspection 812973 - 2012-12-13](https://www.globalkeysolutions.net/api/records/fda_inspections/angiomed-gmbh-co-medizintechnik-kg/5af56e04-5283-4785-b495-96414824469d/)
- [FDA Inspection 812973 - 2012-12-13](https://www.globalkeysolutions.net/api/records/fda_inspections/angiomed-gmbh-co-medizintechnik-kg/75629000-723b-4c32-9864-7b0f34af0435/)

Company: https://www.globalkeysolutions.net/companies/angiomed-gmbh-co-medizintechnik-kg/f65979ce-b9e7-4c49-b3be-5ff000969919

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