# FDA Inspection 1109013 - Paragon BioTeck Inc - September 25, 2019

Source: https://www.keypedia.com/records/fda_inspections/paragon-bioteck-inc/0c351b46-aa52-43b7-a16c-a68f00da30e5
Source feed: FDA_Inspections

> FDA Inspection 1109013 for Paragon BioTeck Inc on September 25, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1109013
- Company Name: Paragon BioTeck Inc
- Inspection Date: 2019-09-25
- 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 1109013 - 2019-09-25](https://www.keypedia.com/records/fda_inspections/paragon-bioteck-inc/47edcba9-61bd-4ece-a199-15198e89477a)
- [FDA Inspection 923477 - 2015-04-03](https://www.keypedia.com/records/fda_inspections/paragon-bioteck-inc/8f581273-702c-4407-b012-834300428f5e)

Company: https://www.keypedia.com/companies/paragon-bioteck-inc/ad55fe7a-7e22-4e9f-bcb2-8c4b00ea0bd9

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