FDA Inspection
Neurolign USA, LlcNeurolign USA, Llc – FDA Inspection, Apr 14, 2016
Record Details
This FDA Inspection record concerns Neurolign USA, Llc, with an inspection on April 14, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Neurolign USA, Llc
- Inspection Date
- April 14, 2016
- Product Type
- Devices
View Company Profile
ID · f476a546-a9d3-4836-baf8-a5e01b0e4e52
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 984418
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: 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 |
| May 17, 2013 | OAI | Center for Devices and Radiological Health | Compliance: Devices |
| April 20, 2010 | 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 832575 - 2013-05-17
- FDA Inspection 657532 - 2010-04-20
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