Company
United StatesNeurotron. Inc., Aurora, CO – FDA Inspections
Inspection records and compliance data for Neurotron. Inc. in Aurora, Colorado. 6 FDA inspections on record, 2 Form 483s, last inspected April 10, 2017.
Company Profile
This profile covers Neurotron. Inc. based in Aurora, Colorado, United States.
FDA Inspection History
- FDA inspections
- 6
- OAI
- 0
- VAI
- 2
- NAI
- 4
- Form 483s
- 2
- Warning letters
- 0
First inspected December 17, 2008. Last inspected April 10, 2017.
Most cited issue areas
- Calibration, Inspection, etc. Procedures Lack of or Inadequ1 inspection
- Lack of or inadequate complaint procedures1 inspection
- Lack of or inadequate receiving acceptance procedures1 inspection
FDA inspections (6)
| Date | Result | FDA center(s) | Insp. # |
|---|---|---|---|
| April 10, 2017 | VAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 1007463 |
| April 10, 2017 | VAI | Medical Devices & Rad Health · Compliance: Devices | 1007462 |
| September 18, 2012 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 799351 |
| September 12, 2012 | NAI | Medical Devices & Rad Health · Compliance: Devices | 798374 |
| September 27, 2010 | NAI | Medical Devices & Rad Health · Postmarket Assurance: Devices | 682551 |
| December 17, 2008 | NAI | Medical Devices & Rad Health · Compliance: Devices | 554398 |
FDA documents
No Form 483s, Warning Letters or EIRs on record.
Related Companies (10)
Companies with similar regulatory profiles, compliance history, and operations.
Company Information
Name
Neurotron. Inc.
FEI Number
1121806
Address
12635 E Montview Blvd Ste 127, Aurora, Colorado 80045, United States
Country
United States
ID: 2f572ad6-cb5f-4096-bd37-b1facb33774c