# FDA Inspection 628201 - Medical Equipment Device Specialists - October 16, 2009

Source: https://www.keypedia.com/records/fda_inspections/medical-equipment-device-specialists/5e726d86-df64-4e65-bbe0-2c1eb9f5a9e0
Source feed: FDA_Inspections

> FDA Inspection 628201 for Medical Equipment Device Specialists on October 16, 2009. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 628201
- Company Name: Medical Equipment Device Specialists
- Inspection Date: 2009-10-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 890741 - 2014-08-06](https://www.keypedia.com/records/fda_inspections/medical-equipment-device-specialists/997fd8e0-5e2c-4f03-bb90-0bea1cfbfcc5)
- [FDA Inspection 890741 - 2014-08-06](https://www.keypedia.com/records/fda_inspections/medical-equipment-device-specialists/562698ac-861a-4f9d-b0c1-2cb5378fb061)

Company: https://www.keypedia.com/companies/medical-equipment-device-specialists/c67b9ea6-9cc7-4fac-aa79-4b344af5b3fd

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