# FDA Inspection 838942 - Barco Inc. - June 13, 2013

Source: https://www.keypedia.com/records/fda_inspections/barco-inc/d6e9d48e-efe7-426a-99a7-fb035429f546
Source feed: FDA_Inspections

> FDA Inspection 838942 for Barco Inc. on June 13, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 838942
- Company Name: Barco Inc.
- Inspection Date: 2013-06-13
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 838942 - 2013-06-13](https://www.keypedia.com/records/fda_inspections/barco-inc/1ff5e178-aa39-40a1-b44f-d39c60a4c37e)
- [FDA Inspection 653135 - 2010-01-22](https://www.keypedia.com/records/fda_inspections/barco-inc/0c31c6f3-fad3-4c7d-a9d7-829d4e75205d)
- [FDA Inspection 653135 - 2010-01-22](https://www.keypedia.com/records/fda_inspections/barco-inc/5153e936-e343-4d21-b4c1-d58399dba520)

Company: https://www.keypedia.com/companies/barco-inc/1b5ff106-54f8-4449-8dc1-59116d1e215a

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