# FDA Inspection 1011997 - Kelyniam Global, Inc. - May 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/kelyniam-global-inc/cfc7c327-117c-47b7-8257-cb3bf6ca6f62
Source feed: FDA_Inspections

> FDA Inspection 1011997 for Kelyniam Global, Inc. on May 30, 2017. Classification: Official Action Indicated (OAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1011997
- Company Name: Kelyniam Global, Inc.
- Inspection Date: 2017-05-30
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1230547 - 2024-08-23](https://www.keypedia.com/records/fda_inspections/kelyniam-global-inc/d6390040-1f05-4e6e-8840-b884901fbd5e)
- [FDA Inspection 1230547 - 2024-08-23](https://www.keypedia.com/records/fda_inspections/kelyniam-global-inc/e394b21d-df36-4022-8ccb-aa9f98900ced)
- [FDA Inspection 1146978 - 2021-07-22](https://www.keypedia.com/records/fda_inspections/kelyniam-global-inc/b2785922-1487-4303-868d-c8a0578d3320)
- [FDA Inspection 1100191 - 2019-08-15](https://www.keypedia.com/records/fda_inspections/kelyniam-global-inc/8becbfdd-bdf2-469b-9329-849d3888b234)
- [FDA Inspection 1066747 - 2018-09-25](https://www.keypedia.com/records/fda_inspections/kelyniam-global-inc/44570904-d1b3-4a76-9559-f9635ac91aa7)

Company: https://www.keypedia.com/companies/kelyniam-global-inc/447b1f6a-d649-4aa2-9115-afbe99879688

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