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BEKA Hospitec Gmbh, Wetzlar, Germany – FDA Inspections

Inspection records and compliance data for BEKA Hospitec Gmbh in Wetzlar. 1 FDA inspection on record, 1 Form 483, last inspected February 02, 2017.

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Company Profile

This profile covers BEKA Hospitec Gmbh based in Wetzlar, Germany.

FDA Inspection History

FDA inspections
1
OAI
0
VAI
1
NAI
0
Form 483s
1
Warning letters
0

Inspected February 2, 2017.

Most cited issue areas

  • Complaints1 inspection
  • Design changes - Lack of or Inadequate Procedures1 inspection
  • Design validation acceptance criteria1 inspection

FDA inspections (1)

DateResultFDA center(s)Insp. #
February 2, 2017VAIMedical Devices & Rad Health · Compliance: Devices1002323
FDA documents

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

Related Companies (10)

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Theodor J. M. Fischlein, MD
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Karl Storz GmbH & Co.
Fiagon GmbH
Siemens Healthcare Diagnostics Products GmbH
Raimund Wenzler Gmbh
Physiomed Elektromedizin AG
Stihler Electronic Gmbh
Company Information

Name

BEKA Hospitec Gmbh

FEI Number

3003878287

Address

Am Rubenmorgen 3, Wetzlar, Germany

Country

Germany

ID: 36e1b5a3-322e-4846-b8d4-19133b4a4165

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