# FDA Inspection 993559 - Bion Enterprises Ltd. - November 18, 2016

Source: https://www.keypedia.com/records/fda_inspections/bion-enterprises-ltd/c893b0b3-47aa-4f87-b2ff-6e2485e2c0b8
Source feed: FDA_Inspections

> FDA Inspection 993559 for Bion Enterprises Ltd. on November 18, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 993559
- Company Name: Bion Enterprises Ltd.
- Inspection Date: 2016-11-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 993559 - 2016-11-18](https://www.keypedia.com/records/fda_inspections/bion-enterprises-ltd/e415d848-eae1-4cd4-a76d-b57b31928356)
- [FDA Inspection 777732 - 2012-04-18](https://www.keypedia.com/records/fda_inspections/bion-enterprises-ltd/225cbb34-0369-4120-9fda-7eb2e9b65b4b)
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- [FDA Inspection 566149 - 2009-03-02](https://www.keypedia.com/records/fda_inspections/bion-enterprises-ltd/00b8e275-1100-4324-83ae-dd08bf1a30a0)

Company: https://www.keypedia.com/companies/bion-enterprises-ltd/98acb389-8381-4feb-ae7d-e0e4810354f3

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