FDA Inspection
Teledyne Flir Commercial Systems, Inc.Teledyne Flir Commercial Systems, Inc. – FDA Inspection, Jul 29, 2015
Record Details
This FDA Inspection record concerns Teledyne Flir Commercial Systems, Inc., with an inspection on July 29, 2015, issued by the Center for Devices and Radiological Health, covering devices.
- Inspection Date
- July 29, 2015
- Product Type
- Devices
View Company Profile
ID · cbe9e307-f976-427b-bcbc-ed8bf9772331
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 939046
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 820.198(a)Lack of or inadequate complaint procedures
- 21 CFR 803.17Lack of Written MDR Procedures
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Teledyne Flir Commercial Systems, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 4, 2022 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 27, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Teledyne Flir Commercial Systems, Inc.
- FDA Inspection 1181787 - 2022-10-04
- FDA Inspection 1058506 - 2018-06-27
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.