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Fehling Instruments GmbH & Co. KG, Karlstein A. Main, Germany – FDA Inspections

Inspection records and compliance data for Fehling Instruments GmbH & Co. KG in Karlstein A. Main. 3 FDA inspections on record (1 OAI), 1 Form 483, 1 warning letter, last inspected March 12, 2026.

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Company Profile

This profile covers Fehling Instruments GmbH & Co. KG based in Karlstein A. Main, Germany.

FDA Inspection History

FDA inspections
3
OAI
1
VAI
0
NAI
1
Unclassified
1
Form 483s
1
Warning letters
1

First inspected June 18, 2015. Last inspected March 12, 2026.

Most cited issue areas

  • Calibration, Inspection, etc. Procedures Lack of or Inadequ1 inspection
  • Design input - Lack of or inadequate procedures1 inspection
  • Design review - Lack of or inadequate procedures1 inspection

FDA inspections (3)

DateResultFDA center(s)Insp. #
March 12, 2026Not classifiedMedical Devices & Rad Health · Compliance: Medical Devices1306904
May 23, 2019NAIMedical Devices & Rad Health · Compliance: Devices1097118
June 18, 2015OAIMedical Devices & Rad Health · Postmarket Assurance: Devices933817
FDA documents

Form 483s (1)

  • Form 483s · August 4, 2022

Warning Letters (1)

  • Warning Letters · June 18, 2015
People (3)
Sean M. Boyd
Person
Peter Skott
Person
Jude C. Dike
Person
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Company Information

Name

Fehling Instruments GmbH & Co. KG

FEI Number

3001286223

Address

Hanauer Landstr. 7a, Karlstein A. Main, Germany

Country

Germany

ID: 5de69c57-56e8-4569-8e3e-8816ce90532e

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