# Remel Europe Ltd. – FDA Inspection, Feb 11, 2016

Source: https://www.keypedia.com/records/fda_inspections/remel-europe-ltd/4adc6293-b298-482d-bd9b-dfabdcd47034
Source feed: FDA_Inspections

> FDA inspection 961738 of Remel Europe Ltd., February 11, 2016. Classification: Official Action Indicated (OAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 961738
- Company Name: Remel Europe Ltd.
- Inspection Date: 2016-02-11
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1116790 - 2019-04-04](https://www.keypedia.com/records/fda_inspections/remel-europe-ltd/a4a99b81-77e9-4448-b3f3-e19826ce71f3)
- [FDA Inspection 840261 - 2013-05-31](https://www.keypedia.com/records/fda_inspections/remel-europe-ltd/4ea1fcbe-92b6-43ad-aa60-1e72cf88e8f4)
- FDA Inspection 580616 - 2009-04-09

Company: https://www.keypedia.com/companies/remel-europe-ltd/c8f6163c-c8ee-4b78-921f-33b58016e464

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