# OSKO, Inc. – FDA Inspection, May 3, 2019

Source: https://www.keypedia.com/records/fda_inspections/osko-inc/c5f936f0-3360-4265-8668-df90f8700b94
Source feed: FDA_Inspections

> FDA inspection 1088391 of OSKO, Inc., May 03, 2019. Classification: Official Action Indicated (OAI). 19 citations under 21 CFR parts 820, 1002, 1003 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: 1088391
- Company Name: OSKO, Inc.
- Inspection Date: 2019-05-03
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 19

## Related Documents

- [FDA Inspection 1022321 - 2017-08-17](https://www.keypedia.com/records/fda_inspections/osko-inc/c7457a05-cec3-4cd4-a32a-304b7f115365)

## Related Officers

- [Investigator](https://www.keypedia.com/people/ashley-a-mutawakkil/512be391-fd96-451c-9569-98e43cfba9db)

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