# FDA Inspection 580616 - Remel Europe Ltd. - April 09, 2009

Source: https://www.keypedia.com/records/fda_inspections/remel-europe-ltd/1fcbbf07-e3bf-4a7e-83c3-e022a2f54041
Source feed: FDA_Inspections

> FDA Inspection 580616 for Remel Europe Ltd. on April 09, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 580616
- Company Name: Remel Europe Ltd.
- Inspection Date: 2009-04-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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