# Remel Europe Ltd., Dartford, United Kingdom – FDA Inspections

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

> Inspection records and compliance data for Remel Europe Ltd. in Dartford. 4 FDA inspections on record (1 OAI), 1 Form 483, last inspected April 04, 2019.

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## Details

- Name: Remel Europe Ltd.
- FEI Number: 3003750284
- Address Line 1: Clipper Boulevard West, Ken
- City: Dartford
- Country Name: United Kingdom
- Address: Clipper Boulevard West, Ken, Dartford, United Kingdom
- Country: United Kingdom

## Related Documents

- [FDA Inspection 1116790 - Remel Europe Ltd. - 2019-04-04](https://www.keypedia.com/records/fda_inspections/remel-europe-ltd/a4a99b81-77e9-4448-b3f3-e19826ce71f3) — source: FDA, date: April 4, 2019
- FDA Inspection 961738 - Remel Europe Ltd. - 2016-02-11 — classification: No Action Indicated (NAI), source: FDA, date: February 11, 2016
- [FDA Inspection 961738 - Remel Europe Ltd. - 2016-02-11](https://www.keypedia.com/records/fda_inspections/remel-europe-ltd/4adc6293-b298-482d-bd9b-dfabdcd47034) — classification: Official Action Indicated (OAI), source: FDA, date: February 11, 2016
- [FDA Inspection 840261 - Remel Europe Ltd. - 2013-05-31](https://www.keypedia.com/records/fda_inspections/remel-europe-ltd/4ea1fcbe-92b6-43ad-aa60-1e72cf88e8f4) — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 31, 2013
- FDA Inspection 580616 - Remel Europe Ltd. - 2009-04-09 — classification: No Action Indicated (NAI), source: FDA, date: April 9, 2009

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