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FDA Inspection
•Mid-Iowa Fertility PC•June 27, 2018

Mid-Iowa Fertility PC – FDA Inspection, Jun 27, 2018

Record Details

This FDA Inspection record concerns Mid-Iowa Fertility PC, with an inspection on June 27, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Mid-Iowa Fertility PC
Inspection Date
June 27, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Eric T. Huebler (Issuing Officer)
View Company Profile

ID · cd26256e-39dc-4082-93e1-0d2492931fc0

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1061152
FDA center
Biologics
Project area
Human Cellular, Tissue, and Gene Therapies

Other FDA inspections of Mid-Iowa Fertility PC

6
DateClassificationOfficeProject area
May 19, 2026NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
September 26, 2023NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
April 12, 2016NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
March 20, 2014NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
November 22, 2011NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
View all 6 other inspections on the company page
Other documents for Mid-Iowa Fertility PC
  • FDA Inspection 1320354 - 2026-05-19
  • FDA Inspection 1220219 - 2023-09-26
  • FDA Inspection 967417 - 2016-04-12
  • FDA Inspection 870631 - 2014-03-20
  • FDA Inspection 754634 - 2011-11-22

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