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Ferrosan Medical Devices, Szczecin, Poland – FDA Inspections

Inspection records and compliance data for Ferrosan Medical Devices in Szczecin. 1 FDA inspection on record, last inspected September 09, 2015.

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Company Profile

This profile covers Ferrosan Medical Devices based in Szczecin, Poland.

FDA Inspection History

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

Inspected September 9, 2015.

FDA inspections (1)

DateResultFDA center(s)Insp. #
September 9, 2015NAIMedical Devices & Rad Health · Compliance: Devices943948
FDA documents

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

Related Companies (10)

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

ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Prof. Rodryg Ramlau, M.D.
LINA MEDICAL POLSKA SP Z.O.O.
Jago-Pro Sp.Z O.O.
Aesculap-Chifa SP. Z.O.O.
CLINICO MEDICAL SP. Z O.O.
MEDICALGORITHMICS S.A.
Raf-Med
DGS Diagnostic Sp. z.o.o.
Waclaw B. Kuczmik, M.D. PhD
Company Information

Name

Ferrosan Medical Devices

FEI Number

3009652348

Address

Ul. Koksowa 3, Szczecin, Poland

Country

Poland

ID: 2fdd3871-ad85-410e-9c11-a8b4a98d181c

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