FDA Inspection
Luminex CorporationLuminex Corporation – FDA Inspection, Apr 6, 2018
Record Details
This FDA Inspection record concerns Luminex Corporation, with an inspection on April 6, 2018, issued by the Dallas District Office, covering medical devices & rad health.
- Company
- Luminex Corporation
- Inspection Date
- April 6, 2018
- Product Type
- Medical Devices & Rad Health
- Office
- Dallas District Office
View Company Profile
ID · 65c698b5-c61f-4be6-8069-1b39f75b1ea8
Inspection Facts
- Inspection number
- 1079277
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Luminex Corporation
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 13, 2023 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 14, 2020 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 15, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 9, 2009 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
Other documents for Luminex Corporation
- FDA Inspection 1195233 - 2023-01-13
- FDA Inspection 1117835 - 2020-02-14
- FDA Inspection 768656 - 2012-02-15
- FDA Inspection 561479 - 2009-02-09
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