# Guidemia Technologies Inc. – FDA Inspection, Jul 3, 2017

Source: https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/30e549ec-ae05-4528-94a8-ff28886dd23b
Source feed: FDA_Inspections

> FDA inspection 1021559 of Guidemia Technologies Inc., July 03, 2017. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1021559
- Company Name: Guidemia Technologies Inc.
- Inspection Date: 2017-07-03
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Los Angeles District Office
- Citation Count: 0

## Related Documents

- [FDA Inspection 1325530 - 2026-07-06](https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/db5d20bc-23f8-4387-8e18-4f46d7dcf127)
- FDA Inspection 1081235 - 2019-02-11
- [FDA Inspection 859270 - 2013-12-12](https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/ff06699e-4f86-435c-8205-b3bdbee07fb2)

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/guidemia-technologies-inc/a4f32aed-30e9-49cb-a1e2-6efe08778b58

Office: https://www.keypedia.com/offices/los-angeles-district-office/edcf1dfe-596a-43b8-8df4-07d9cd94763b