# FDA Inspection 1088391 - OSKO, Inc. - May 03, 2019

Source: https://www.keypedia.com/records/fda_inspections/osko-inc/5a61235e-5527-417d-bf4d-08e39e3e86c7
Source feed: FDA_Inspections

> FDA Inspection 1088391 for OSKO, Inc. on May 03, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1088391
- Company Name: OSKO, Inc.
- Inspection Date: 2019-05-03
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1088391 - 2019-05-03](https://www.keypedia.com/records/fda_inspections/osko-inc/574348c8-022e-41f7-b283-be1162535880)
- [FDA Inspection 1088391 - 2019-05-03](https://www.keypedia.com/records/fda_inspections/osko-inc/c5f936f0-3360-4265-8668-df90f8700b94)
- [FDA Inspection 1022321 - 2017-08-17](https://www.keypedia.com/records/fda_inspections/osko-inc/c7457a05-cec3-4cd4-a32a-304b7f115365)
- [FDA Inspection 1022321 - 2017-08-17](https://www.keypedia.com/records/fda_inspections/osko-inc/63b56a7f-6088-429c-ae9a-0a81e10922d9)
- [FDA Inspection 1022321 - 2017-08-17](https://www.keypedia.com/records/fda_inspections/osko-inc/6129e86a-1530-45ec-a698-7532851a7e1b)

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