# FDA Inspection 965120 - Avery Dennison Corp/Avery Dennison Medical - March 11, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/avery-dennison-corpavery-dennison-medical/fe8928a3-5f4b-4b44-8011-8f63365428ca/
Source feed: FDA_Inspections

> FDA Inspection 965120 for Avery Dennison Corp/Avery Dennison Medical on March 11, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 965120
- Company Name: Avery Dennison Corp/Avery Dennison Medical
- Inspection Date: 2016-03-11
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 965120 - 2016-03-11](https://www.globalkeysolutions.net/api/records/fda_inspections/avery-dennison-corpavery-dennison-medical/a76e6f56-45cc-4cfd-8167-6f1d05f44ce2/)

Company: https://www.globalkeysolutions.net/companies/avery-dennison-corpavery-dennison-medical/4b50122e-f7ad-45c6-b314-ef1f190bc6be

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