# FDA Inspection 823554 - Edlo S/A Medical Products - March 07, 2013

Source: https://www.keypedia.com/records/fda_inspections/edlo-sa-medical-products/7fe2590e-8d27-4d5a-ae88-f403c12f2af8
Source feed: FDA_Inspections

> FDA Inspection 823554 for Edlo S/A Medical Products on March 07, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 823554
- Company Name: Edlo S/A Medical Products
- 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

## Related Documents

- [FDA Inspection 823554 - 2013-03-07](https://www.keypedia.com/records/fda_inspections/edlo-sa-medical-products/3d074f67-b344-4f21-9391-0f3b055a3771)

Company: https://www.keypedia.com/companies/edlo-sa-medical-products/55df3a93-b991-4266-86e9-854d7a344718

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