# Kessel Medintim Gmbh – FDA Inspection, Nov 2, 2017

Source: https://www.keypedia.com/records/fda_inspections/kessel-medintim-gmbh/9d4bd2ea-5bff-46d9-afe5-6eefe6914bbd
Source feed: FDA_Inspections

> FDA inspection 1030511 of Kessel Medintim Gmbh, November 02, 2017. 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1030511
- Company Name: Kessel Medintim Gmbh
- Inspection Date: 2017-11-02
- Project Area: Compliance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Office of Inspections and Investigations
- Citation Count: 1

## Related Officers

- Issuing Officer

Company: https://www.keypedia.com/companies/kessel-medintim-gmbh/d7f07554-63d8-4ded-9f9c-6bd420fa5caf

Office: https://www.keypedia.com/offices/office-of-inspections-and-investigations/7dd0b904-a3df-46bc-a7b2-70ddb6f809c8