# FDA Inspection 1063765 - Opus KSD, Inc. - August 15, 2018

Source: https://www.keypedia.com/records/fda_inspections/opus-ksd-inc/736a0e3a-3c35-45f4-af32-2d29a0950196
Source feed: FDA_Inspections

> FDA Inspection 1063765 for Opus KSD, Inc. on August 15, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063765
- Company Name: Opus KSD, Inc.
- Inspection Date: 2018-08-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1156653 - 2021-11-12](https://www.keypedia.com/records/fda_inspections/opus-ksd-inc/4742718b-0f22-4bc4-b272-eff291e0da3f)
- [FDA Inspection 1156653 - 2021-11-12](https://www.keypedia.com/records/fda_inspections/opus-ksd-inc/1b0ca7b8-7bc1-4a9d-9199-f190eb05849c)

Company: https://www.keypedia.com/companies/opus-ksd-inc/a8c6b9ca-5b92-4a2a-b2a8-1a3c9c857320

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