FDA Inspection
Enterix, Inc.Enterix, Inc. – FDA Inspection, Aug 18, 2016
Record Details
This FDA Inspection record concerns Enterix, Inc., with an inspection on August 18, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Enterix, Inc.
- Inspection Date
- August 18, 2016
- Product Type
- Devices
View Company Profile
ID · 38839f21-7b54-402c-a935-6f1107afd7a0
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 983532
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
Other FDA inspections of Enterix, Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| August 10, 2026 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| March 10, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 27, 2012 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| July 1, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Enterix, Inc.
- FDA Inspection 1330540 - 2026-08-10
- FDA Inspection 1199942 - 2023-03-10
- FDA Inspection 808178 - 2012-11-27
- FDA Inspection 670927 - 2010-07-01
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