# FDA Inspection 1089189 - Wykle, Inc. - May 10, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/wykle-inc/540629a9-9f41-40f1-a806-4bface0d023d
Source feed: FDA_Inspections

> FDA Inspection 1089189 for Wykle, Inc. on May 10, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1089189
- Company Name: Wykle, Inc.
- Inspection Date: 2019-05-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1089189 - 2019-05-10](https://www.globalkeysolutions.net/records/fda_inspections/wykle-inc/bb4a96ee-d001-4c56-af42-35f2114eacfe)
- [FDA Inspection 905906 - 2014-11-26](https://www.globalkeysolutions.net/records/fda_inspections/wykle-inc/f41c9695-c9b8-4f90-aef7-9581aaf393fa)
- [FDA Inspection 905906 - 2014-11-26](https://www.globalkeysolutions.net/records/fda_inspections/wykle-inc/f1f902db-8671-4ae9-ba31-8e80da957381)

Company: https://www.globalkeysolutions.net/companies/wykle-inc/f6ee1bfe-7623-4861-a259-0341e0f1412d

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