# FDA Inspection 1061002 - Ontex Hygieneneartikel Gmbh - June 21, 2018

Source: https://www.keypedia.com/records/fda_inspections/ontex-hygieneneartikel-gmbh/aec629d2-af51-417f-ae02-7ffe4f1d1edf
Source feed: FDA_Inspections

> FDA Inspection 1061002 for Ontex Hygieneneartikel Gmbh on June 21, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1061002
- Company Name: Ontex Hygieneneartikel Gmbh
- Inspection Date: 2018-06-21
- 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 1061002 - 2018-06-21](https://www.keypedia.com/records/fda_inspections/ontex-hygieneneartikel-gmbh/97332af9-ebac-43bb-a209-786d669fd33d)
- [FDA Inspection 898920 - 2014-09-18](https://www.keypedia.com/records/fda_inspections/ontex-hygieneneartikel-gmbh/397c0608-f330-4751-8520-83d0788bd269)
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- [FDA Inspection 830498 - 2013-04-11](https://www.keypedia.com/records/fda_inspections/ontex-hygieneneartikel-gmbh/ee137954-8bc1-4b36-9f55-ae928e04f253)

Company: https://www.keypedia.com/companies/ontex-hygieneneartikel-gmbh/c30d9b97-f682-4cef-8524-3edb684a51ee

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