# FDA Inspection 926999 - Integrum Ab - May 21, 2015

Source: https://www.keypedia.com/records/fda_inspections/integrum-ab/d6bb7997-5f6b-4aba-ad41-5ea702064e26
Source feed: FDA_Inspections

> FDA Inspection 926999 for Integrum Ab on May 21, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 926999
- Company Name: Integrum Ab
- Inspection Date: 2015-05-21
- Classification: Voluntary Action Indicated (VAI)
- 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/integrum-ab/de8ad86d-bba0-42ee-ae40-eedadbbfdf5c

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