# FDA Inspection 1027670 - Dreve Otoplastik Gmbh - September 07, 2017

Source: https://www.keypedia.com/records/fda_inspections/dreve-otoplastik-gmbh/faeaed01-6283-4510-81d0-b5f2c7514f0c
Source feed: FDA_Inspections

> FDA Inspection 1027670 for Dreve Otoplastik Gmbh on September 07, 2017. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1027670
- Company Name: Dreve Otoplastik Gmbh
- Inspection Date: 2017-09-07
- Classification: Official Action Indicated (OAI)
- Project Area: Drug Quality Assurance
- Product Type: Drugs
- Office Name: Center for Drug Evaluation and Research

## Related Documents

- [FDA Inspection 894893 - 2014-08-21](https://www.keypedia.com/records/fda_inspections/dreve-otoplastik-gmbh/00cfeefc-49e0-4a89-879a-ae1a0f6d122d)

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

Office: https://www.keypedia.com/offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c