# FDA Inspection 1017153 - Spectros Medical Devices Inc - May 08, 2017

Source: https://www.keypedia.com/records/fda_inspections/spectros-medical-devices-inc/c22bc902-56a9-4b81-a723-caf5a4fcaea9
Source feed: FDA_Inspections

> FDA Inspection 1017153 for Spectros Medical Devices Inc on May 08, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1017153
- Company Name: Spectros Medical Devices Inc
- Inspection Date: 2017-05-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1017153 - 2017-05-08](https://www.keypedia.com/records/fda_inspections/spectros-medical-devices-inc/cd4a15f4-5994-462a-b9db-f9d79174f98f)
- [FDA Inspection 862095 - 2014-01-15](https://www.keypedia.com/records/fda_inspections/spectros-medical-devices-inc/97b3c3bd-579b-44bf-b430-271335c6ba68)
- [FDA Inspection 862095 - 2014-01-15](https://www.keypedia.com/records/fda_inspections/spectros-medical-devices-inc/939c2bcc-fed3-45e6-a67f-3ce25541a6da)

Company: https://www.keypedia.com/companies/spectros-medical-devices-inc/0b478beb-3ad3-4bea-8f9e-832db4d7cd21

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