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Ermis MedTech GmbH, Tuttlingen, Germany – FDA Inspections

Inspection records and compliance data for Ermis MedTech GmbH in Tuttlingen. 2 FDA inspections on record, last inspected June 12, 2024.

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Company Profile

This profile covers Ermis MedTech GmbH based in Tuttlingen, Germany.

FDA Inspection History

FDA inspections
2
OAI
0
VAI
0
NAI
2
Form 483s
0
Warning letters
0

First inspected August 29, 2019. Last inspected June 12, 2024.

FDA inspections (2)

DateResultFDA center(s)Insp. #
June 12, 2024NAIMedical Devices & Rad Health · Compliance: Devices1243750
August 29, 2019NAIMedical Devices & Rad Health · Compliance: Devices1102918
FDA documents

No Form 483s, Warning Letters or EIRs on record.

Related Companies (10)

Companies with similar regulatory profiles, compliance history, and operations.

Stihler Electronic Gmbh
PHS Medical GmbH
Theodor J. M. Fischlein, MD
Spiegelberg Gmbh & Co. KG
German Medical Engineering Gmbh
Elexxion AG
Karl Storz GmbH & Co.
Fiagon GmbH
Siemens Healthcare Diagnostics Products GmbH
Raimund Wenzler Gmbh
Company Information

Name

Ermis MedTech GmbH

FEI Number

3005071827

Address

Dornierstr. 49, Tuttlingen, Germany

Country

Germany

ID: 1e5015c2-2a29-4569-a0af-3d55cf638cc4

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