Kazimierz Kuliczkowski, M.D.

Form 483

Wroclaw, -, PolandFEI 3011759280Issued September 18, 2015

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 3011759280.

Observations2

Issue DateSeptember 18, 2015

StatusNo Warning Letter

Related Inspections3

Establishment Details

Firm: Kazimierz Kuliczkowski, M.D.
Location: Wroclaw, -, Poland
FEI Number: 3011759280
Product Type: Biologics
Issue Date: September 18, 2015
Country: Poland

Inspection History, 2015 to 2019

NAI2

VAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated.

Act on This Form 483

FDA Inspection ReadinessSee how your operations would hold up to the same scrutiny.CAPA & InvestigationsScore how you would investigate and close findings like these.Talk to a SpecialistWalk through these observations with a ComplianceQuest expert.

Kazimierz Kuliczkowski, M.D. FDA Form 483, Wroclaw, September 18, 2015