# FDA Inspection 1109721 - Vertera Inc - September 26, 2019

Source: https://www.keypedia.com/records/fda_inspections/vertera-inc/c93f4c35-6ba9-4946-a8d0-066cadcfdc81
Source feed: FDA_Inspections

> FDA Inspection 1109721 for Vertera Inc on September 26, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1109721
- Company Name: Vertera Inc
- Inspection Date: 2019-09-26
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/vertera-inc/bf261ab0-319d-4aec-989c-48bb0a9c3727

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