# FDA Inspection 1086603 - Hepatiq, Inc. - March 07, 2019

Source: https://www.keypedia.com/records/fda_inspections/hepatiq-inc/535f723b-4eac-4407-a1a2-4e1afef3f9b8
Source feed: FDA_Inspections

> FDA Inspection 1086603 for Hepatiq, Inc. on March 07, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1086603
- Company Name: Hepatiq, Inc.
- Inspection Date: 2019-03-07
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 1211042 - 2023-07-12](https://www.keypedia.com/records/fda_inspections/hepatiq-inc/a091c4e1-561a-476a-ac0f-5024c3152866)
- [FDA Inspection 1086603 - 2019-03-07](https://www.keypedia.com/records/fda_inspections/hepatiq-inc/40854bce-af5e-4878-9c5e-ed2fde9a0783)

Company: https://www.keypedia.com/companies/hepatiq-inc/2e3a917d-d929-471f-a88c-2344d0780876

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