# OSKO, Inc. – FDA Inspection, Aug 17, 2017

Source: https://www.keypedia.com/records/fda_inspections/osko-inc/c7457a05-cec3-4cd4-a32a-304b7f115365
Source feed: FDA_Inspections

> FDA inspection 1022321 of OSKO, Inc., August 17, 2017. Classification: Voluntary Action Indicated (VAI). 9 citations under 21 CFR parts 820, 1002 and 1020. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022321
- Company Name: OSKO, Inc.
- Inspection Date: 2017-08-17
- 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: 9

## Related Documents

- [FDA Inspection 1088391 - 2019-05-03](https://www.keypedia.com/records/fda_inspections/osko-inc/c5f936f0-3360-4265-8668-df90f8700b94)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stanley-b-eugene/4708f43e-0592-4c24-b276-d9f9092788a3)

Company: https://www.keypedia.com/companies/osko-inc/59db7c12-ecc1-42f9-b116-ae61a9d585a2

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