# FDA Inspection 886885 - Mentor Worldwide LLC - June 13, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/mentor-worldwide-llc/6368c606-f045-4680-9ddc-049e852e0b41
Source feed: FDA_Inspections

> FDA Inspection 886885 for Mentor Worldwide LLC on June 13, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 886885
- Company Name: Mentor Worldwide LLC
- Inspection Date: 2014-06-13
- 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 1083046 - 2019-02-07](https://www.globalkeysolutions.net/records/fda_inspections/mentor-worldwide-llc/c41a812c-c0dc-450b-a158-7c75b1013a63)
- [FDA Inspection 613068 - 2009-08-28](https://www.globalkeysolutions.net/records/fda_inspections/mentor-worldwide-llc/12f20f68-38e3-4ba0-9956-49f173871174)

Company: https://www.globalkeysolutions.net/companies/mentor-worldwide-llc/0a2b602b-2e24-4659-9bd5-0b364d58bed2

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