# FDA Inspection 1199942 - Enterix, Inc. - March 10, 2023

Source: https://www.globalkeysolutions.net/records/fda_inspections/enterix-inc/10b41351-4d2c-4ea2-886d-5cc455fddf6c
Source feed: FDA_Inspections

> FDA Inspection 1199942 for Enterix, Inc. on March 10, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199942
- Company Name: Enterix, Inc.
- Inspection Date: 2023-03-10
- 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 1199942 - 2023-03-10](https://www.globalkeysolutions.net/records/fda_inspections/enterix-inc/71ff7d28-02c3-4cd6-9210-4000ccacf182)
- [FDA Inspection 983532 - 2016-08-18](https://www.globalkeysolutions.net/records/fda_inspections/enterix-inc/2e5f6310-8c9b-4623-88fa-78d4ddb67be1)
- [FDA Inspection 983532 - 2016-08-18](https://www.globalkeysolutions.net/records/fda_inspections/enterix-inc/38839f21-7b54-402c-a935-6f1107afd7a0)
- [FDA Inspection 808178 - 2012-11-27](https://www.globalkeysolutions.net/records/fda_inspections/enterix-inc/a469cfd5-1a6d-425d-98a5-9828a9d66c86)
- [FDA Inspection 808178 - 2012-11-27](https://www.globalkeysolutions.net/records/fda_inspections/enterix-inc/cc3921d9-2c3b-4c82-b9cc-2094002c5ceb)

Company: https://www.globalkeysolutions.net/companies/enterix-inc/f801ccab-bedf-4ec7-ab7e-57d65fed2a66

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