# Integrum Ab – FDA Inspection, Sep 8, 2022

Source: https://www.keypedia.com/records/fda_inspections/integrum-ab/f4d1a67e-a5ee-469c-b105-78bd7a398df5
Source feed: FDA_Inspections

> FDA inspection 1180268 of Integrum Ab, September 08, 2022. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1180268
- Company Name: Integrum Ab
- Inspection Date: 2022-09-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1063704 - 2018-08-29](https://www.keypedia.com/records/fda_inspections/integrum-ab/a148b8f5-c13d-4eea-bfec-7008d38c1f63)
- FDA Inspection 926999 - 2015-05-21

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