# FDA Inspection 620258 - Remel Atlanta, A Div. of Remel, Inc. - September 22, 2009

Source: https://www.keypedia.com/records/fda_inspections/remel-atlanta-a-div-of-remel-inc/80798596-4b4e-4eeb-89e5-ad1cecc3efb4
Source feed: FDA_Inspections

> FDA Inspection 620258 for Remel Atlanta, A Div. of Remel, Inc. on September 22, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 620258
- Company Name: Remel Atlanta, A Div. of Remel, Inc.
- Inspection Date: 2009-09-22
- 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-atlanta-a-div-of-remel-inc/b9c2d262-e6c1-4ad0-a0f2-674beb4000ec

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