# FDA Inspection 931135 - Avery Dennison Belgie BV - April 23, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/avery-dennison-belgie-bv/e5d65398-13f7-4a7b-8930-8286b1c97d0f
Source feed: FDA_Inspections

> FDA Inspection 931135 for Avery Dennison Belgie BV on April 23, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 931135
- Company Name: Avery Dennison Belgie BV
- Inspection Date: 2015-04-23
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 931135 - 2015-04-23](https://www.globalkeysolutions.net/records/fda_inspections/avery-dennison-belgie-bv/1c0aea07-1b1b-4886-9e25-567f626ac95a)

Company: https://www.globalkeysolutions.net/companies/avery-dennison-belgie-bv/ea71f6af-4bb3-4158-8375-0b29b87a969e

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