# FDA Inspection 1330540 - Enterix, Inc. - August 10, 2026

Source: https://www.keypedia.com/records/fda_inspections/enterix-inc/b60400db-722e-4183-bbe6-ee3ae328d520
Source feed: FDA_Inspections

> FDA Inspection 1330540 for Enterix, Inc. on August 10, 2026. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1330540
- Company Name: Enterix, Inc.
- Inspection Date: 2026-08-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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