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Goetze-Niemer Co Inc, Kansas City, MO – FDA Inspections

Inspection records and compliance data for Goetze-Niemer Co Inc in Kansas City, Missouri. 4 FDA inspections on record, last inspected February 05, 2020.

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Company Profile

This profile covers Goetze-Niemer Co Inc based in Kansas City, Missouri, United States.

FDA Inspection History

FDA inspections
4
OAI
0
VAI
2
NAI
2
Form 483s
0
Warning letters
0

First inspected March 19, 2014. Last inspected February 5, 2020.

Most cited issue areas

  • Calibration procedures and schedules (general)1 inspection
  • Procedures re complaints1 inspection
  • Procedures to meet core CTGP1 inspection

FDA inspections (4)

DateResultFDA center(s)Insp. #
February 5, 2020NAIBiologics · Human Cellular, Tissue, and Gene Therapies1119118
March 8, 2018NAIBiologics · Blood and Blood Products1044414
December 14, 2015VAIBiologics · Human Cellular, Tissue, and Gene Therapies952168
March 19, 2014VAIBiologics · Human Cellular, Tissue, and Gene Therapies870748
FDA documents

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

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Company Information

Name

Goetze-Niemer Co Inc

FEI Number

3002177077

Address

3939 Ne 33rd Ter Ste J, Kansas City, Missouri 64117, United States

Country

United States

ID: 83703be0-a538-4566-9e96-3f3201ddad4a

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Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
🇺🇸+1 917-789-5099
🇪🇺+48 532-447-507
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