# Guidemia Technologies Inc. – FDA Inspection, Dec 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/guidemia-technologies-inc/ff06699e-4f86-435c-8205-b3bdbee07fb2
Source feed: FDA_Inspections

> FDA inspection 859270 of Guidemia Technologies Inc., December 12, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 803 and 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 859270
- Company Name: Guidemia Technologies Inc.
- Inspection Date: 2013-12-12
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

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- FDA Inspection 1081235 - 2019-02-11
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Company: https://www.keypedia.com/companies/guidemia-technologies-inc/a4f32aed-30e9-49cb-a1e2-6efe08778b58

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7