# FDA Inspection 897713 - Snyder Industries Bensenville - August 08, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/snyder-industries-bensenville/65797adb-2372-4ad6-8093-92b9f66544dc
Source feed: FDA_Inspections

> FDA Inspection 897713 for Snyder Industries Bensenville on August 08, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 897713
- Company Name: Snyder Industries Bensenville
- Inspection Date: 2014-08-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1044306 - 2018-03-14](https://www.globalkeysolutions.net/records/fda_inspections/snyder-industries-bensenville/55a1da0b-4f3d-4300-972d-a9540c54f9aa)
- [FDA Inspection 1044306 - 2018-03-14](https://www.globalkeysolutions.net/records/fda_inspections/snyder-industries-bensenville/6308125a-757e-4d50-9f35-4cd32b21eae1)
- [FDA Inspection 897713 - 2014-08-08](https://www.globalkeysolutions.net/records/fda_inspections/snyder-industries-bensenville/eedebf19-fd82-4c11-906a-b5733889fa8c)

Company: https://www.globalkeysolutions.net/companies/snyder-industries-bensenville/192429bb-4e49-43b0-9fe8-db386bcc755e

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