# FDA Inspection 666928 - Medro Systems, Inc - June 04, 2010

Source: https://www.keypedia.com/records/fda_inspections/medro-systems-inc/38ef20ee-a245-4b56-9d30-36ef23cdf922
Source feed: FDA_Inspections

> FDA Inspection 666928 for Medro Systems, Inc on June 04, 2010. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 666928
- Company Name: Medro Systems, Inc
- Inspection Date: 2010-06-04
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 811185 - 2012-12-18](https://www.keypedia.com/records/fda_inspections/medro-systems-inc/4a4a6102-9217-4ed5-b67b-ec8a5631923d)
- [FDA Inspection 811185 - 2012-12-18](https://www.keypedia.com/records/fda_inspections/medro-systems-inc/b777e337-df96-4f46-990b-c16b75916f30)
- [FDA Inspection 666928 - 2010-06-04](https://www.keypedia.com/records/fda_inspections/medro-systems-inc/7701e221-bdd0-4a84-8c11-bab6340a177c)

Company: https://www.keypedia.com/companies/medro-systems-inc/bae2b862-710a-4b33-bc06-780a3c8b5453

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