# KEOS LLC – FDA Inspection, Aug 23, 2019

Source: https://www.keypedia.com/records/fda_inspections/keos-llc/72908851-263f-48e0-b0de-0a09d6feeefe
Source feed: FDA_Inspections

> FDA inspection 1100408 of KEOS LLC, August 23, 2019. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1100408
- Company Name: KEOS LLC
- Inspection Date: 2019-08-23
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 1196580 - 2023-01-11

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jacob-m-dyer/e3ca27e3-e0b1-4db8-9cbe-cfaff90b83cf)

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