# FDA Inspection 871103 - Medtronic Virginia Beach - March 20, 2014

Source: https://www.globalkeysolutions.net/records/fda_inspections/medtronic-virginia-beach/c951a04a-809c-4099-a547-14c2b428ba38
Source feed: FDA_Inspections

> FDA Inspection 871103 for Medtronic Virginia Beach on March 20, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 871103
- Company Name: Medtronic Virginia Beach
- Inspection Date: 2014-03-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 871103 - 2014-03-20](https://www.globalkeysolutions.net/records/fda_inspections/medtronic-virginia-beach/02e8a2a2-4e88-4c89-a98c-fe2fca0ba398)
- [FDA Inspection 756727 - 2011-12-12](https://www.globalkeysolutions.net/records/fda_inspections/medtronic-virginia-beach/dc41ea63-e949-4ed7-b97f-f0e93c7ce284)

Company: https://www.globalkeysolutions.net/companies/medtronic-virginia-beach/4e7fbd37-c661-4dc0-aab9-998fd53fe2e8

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