FDA Inspection
Neurolign USA, LlcNeurolign USA, Llc – FDA Inspection, May 17, 2013
Record Details
This FDA Inspection record concerns Neurolign USA, Llc, with an inspection on May 17, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Neurolign USA, Llc
- Inspection Date
- May 17, 2013
- Product Type
- Devices
View Company Profile
ID · fc8602b5-5b82-4332-9eac-83af2641eb03
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 832575
- 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 |
| 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 984418 - 2016-04-14
- FDA Inspection 657532 - 2010-04-20
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