# FDA Inspection 1105962 - InterValve Medical, Inc - September 12, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/intervalve-medical-inc/fb772af6-7dfc-4453-9890-0b0dec26372a/
Source feed: FDA_Inspections

> FDA Inspection 1105962 for InterValve Medical, Inc on September 12, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1105962
- Company Name: InterValve Medical, Inc
- Inspection Date: 2019-09-12
- 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 1105962 - 2019-09-12](https://www.globalkeysolutions.net/api/records/fda_inspections/intervalve-medical-inc/c7f73b0d-e9e3-4998-8de9-e0f2c14d0896/)
- [FDA Inspection 874413 - 2014-04-02](https://www.globalkeysolutions.net/api/records/fda_inspections/intervalve-medical-inc/bbc40156-1853-43f1-8d7d-3888a38cd639/)

Company: https://www.globalkeysolutions.net/companies/intervalve-medical-inc/2190ef60-9ced-4e31-9978-dc31a51c5dc0

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