# Enterix, Inc. – FDA Inspection, Mar 10, 2023

Source: https://www.keypedia.com/records/fda_inspections/enterix-inc/71ff7d28-02c3-4cd6-9210-4000ccacf182
Source feed: FDA_Inspections

> FDA inspection 1199942 of Enterix, Inc., March 10, 2023. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199942
- Company Name: Enterix, Inc.
- Inspection Date: 2023-03-10
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1330540 - 2026-08-10](https://www.keypedia.com/records/fda_inspections/enterix-inc/b60400db-722e-4183-bbe6-ee3ae328d520)
- [FDA Inspection 983532 - 2016-08-18](https://www.keypedia.com/records/fda_inspections/enterix-inc/38839f21-7b54-402c-a935-6f1107afd7a0)
- FDA Inspection 808178 - 2012-11-27
- FDA Inspection 670927 - 2010-07-01

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/frank-j-marciniak/6995351a-6afc-4056-9692-d4aeb711dd92)

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