# FDA Inspection 823206 - Remel, Inc - March 07, 2013

Source: https://www.keypedia.com/records/fda_inspections/remel-inc/009c8ef8-abeb-4512-9d42-ff06f1f7eaba
Source feed: FDA_Inspections

> FDA Inspection 823206 for Remel, Inc on March 07, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 823206
- Company Name: Remel, Inc
- Inspection Date: 2013-03-07
- 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-inc/f75612ef-610e-4ee4-980b-47569a492300

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