FDA Inspection
Neurolign USA, LlcNeurolign USA, Llc – FDA Inspection, Apr 20, 2010
Record Details
This FDA Inspection record concerns Neurolign USA, Llc, with an inspection on April 20, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Neurolign USA, Llc
- Inspection Date
- April 20, 2010
- Product Type
- Devices
View Company Profile
ID · 57dc1d0f-a991-4814-80c3-d1f4abf95714
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 657532
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Neurolign USA, Llc
5| Date | Classification | Office | Project area |
|---|---|---|---|
| February 25, 2025 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| October 13, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 2, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| April 14, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| May 17, 2013 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Neurolign USA, Llc
- FDA Inspection 1262634 - 2025-02-25
- FDA Inspection 1181451 - 2022-10-13
- FDA Inspection 1095111 - 2019-07-02
- FDA Inspection 984418 - 2016-04-14
- FDA Inspection 832575 - 2013-05-17
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