# FDA Inspection 1082136 - OEHM UND REHBEIN GMBH - January 17, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/oehm-und-rehbein-gmbh/9b0badbb-afe9-4fbc-8e02-b5e144ca8ee0
Source feed: FDA_Inspections

> FDA Inspection 1082136 for OEHM UND REHBEIN GMBH on January 17, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1082136
- Company Name: OEHM UND REHBEIN GMBH
- Inspection Date: 2019-01-17
- 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 1082136 - 2019-01-17](https://www.globalkeysolutions.net/records/fda_inspections/oehm-und-rehbein-gmbh/d37a0f19-a8c6-4f14-a055-a2bd5e222459)

Company: https://www.globalkeysolutions.net/companies/oehm-und-rehbein-gmbh/b0717aa6-d788-438e-b5d1-d0a238e43ecb

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