# FDA Inspection 580625 - Prostalund AB - April 17, 2009

Source: https://www.keypedia.com/records/fda_inspections/prostalund-ab/cc5ccd43-010b-4294-90e7-9f2ac2742e13
Source feed: FDA_Inspections

> FDA Inspection 580625 for Prostalund AB on April 17, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 580625
- Company Name: Prostalund AB
- Inspection Date: 2009-04-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/prostalund-ab/69b2cde7-4d18-4ea6-afde-3ddc627500af

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