# FDA Inspection 961291 - Perimed AB - February 11, 2016

Source: https://www.keypedia.com/records/fda_inspections/perimed-ab/08aab5df-0c9a-449a-8475-194bfadb9e45
Source feed: FDA_Inspections

> FDA Inspection 961291 for Perimed AB on February 11, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 961291
- Company Name: Perimed AB
- Inspection Date: 2016-02-11
- 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/perimed-ab/c2877ac7-60d3-41f5-8934-2d153968829e

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