FDA Inspection
Guidemia Technologies Inc.Guidemia Technologies Inc. – FDA Inspection, Jul 3, 2017
Record Details
This FDA Inspection record concerns Guidemia Technologies Inc., with an inspection on July 3, 2017, issued by the Los Angeles District Office, covering medical devices & rad health.
- Company
- Guidemia Technologies Inc.
- Inspection Date
- July 3, 2017
- Product Type
- Medical Devices & Rad Health
- Person
- CNTRMMNTR MAGEET (Issuing Officer)
View Company Profile
ID · 30e549ec-ae05-4528-94a8-ff28886dd23b
Inspection Facts
- Inspection number
- 1021559
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Guidemia Technologies Inc.
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 6, 2026 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| February 11, 2019 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| December 12, 2013 | VAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Guidemia Technologies Inc.
- FDA Inspection 1325530 - 2026-07-06
- FDA Inspection 1081235 - 2019-02-11
- FDA Inspection 859270 - 2013-12-12
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