# FDA Inspection 1196580 - KEOS LLC - January 11, 2023

Source: https://www.keypedia.com/records/fda_inspections/keos-llc/41b3cf36-678b-48e4-a188-b06d4acdaa74
Source feed: FDA_Inspections

> FDA Inspection 1196580 for KEOS LLC on January 11, 2023. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1196580
- Company Name: KEOS LLC
- Inspection Date: 2023-01-11
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1196580 - 2023-01-11](https://www.keypedia.com/records/fda_inspections/keos-llc/1dcd1023-fbbf-437a-b6df-176311faa329)
- [FDA Inspection 1100408 - 2019-08-23](https://www.keypedia.com/records/fda_inspections/keos-llc/72908851-263f-48e0-b0de-0a09d6feeefe)

Company: https://www.keypedia.com/companies/keos-llc/46e19ba4-a420-4ecf-a317-0e59efaefa22

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