# IT Dr. Gambert Gmbh – FDA Inspection, Jan 27, 2011

Source: https://www.keypedia.com/records/fda_inspections/it-dr-gambert-gmbh/7e25c3cd-0c3b-4209-ace3-0d2f4cc37a41
Source feed: FDA_Inspections

> FDA inspection 709723 of IT Dr. Gambert Gmbh, January 27, 2011. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 709723
- Company Name: IT Dr. Gambert Gmbh
- Inspection Date: 2011-01-27
- 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: 7

Company: https://www.keypedia.com/companies/it-dr-gambert-gmbh/4611881e-3571-4be1-b097-2462641f912a

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