# FDA Inspection 894893 - Dreve Otoplastik Gmbh - August 21, 2014

Source: https://www.keypedia.com/records/fda_inspections/dreve-otoplastik-gmbh/00cfeefc-49e0-4a89-879a-ae1a0f6d122d
Source feed: FDA_Inspections

> FDA Inspection 894893 for Dreve Otoplastik Gmbh on August 21, 2014. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 894893
- Company Name: Dreve Otoplastik Gmbh
- Inspection Date: 2014-08-21
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1027670 - 2017-09-07](https://www.keypedia.com/records/fda_inspections/dreve-otoplastik-gmbh/faeaed01-6283-4510-81d0-b5f2c7514f0c)

Company: https://www.keypedia.com/companies/dreve-otoplastik-gmbh/c04ff831-b4ff-471b-a5b1-036065c6f59a

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