# Remel Europe Ltd. – FDA Inspection, Apr 4, 2019

Source: https://www.keypedia.com/records/fda_inspections/remel-europe-ltd/a4a99b81-77e9-4448-b3f3-e19826ce71f3
Source feed: FDA_Inspections

> FDA inspection 1116790 of Remel Europe Ltd., April 04, 2019. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1116790
- Company Name: Remel Europe Ltd.
- Inspection Date: 2019-04-04
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 0

## Related Documents

- [FDA Inspection 961738 - 2016-02-11](https://www.keypedia.com/records/fda_inspections/remel-europe-ltd/4adc6293-b298-482d-bd9b-dfabdcd47034)
- [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/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8