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FDA Inspection
•Christopher T.F. Huang M.D., Inc. dba Advanced Reproductive Center of Hawaii•August 10, 2018

Christopher T.F. Huang M.D., Inc. dba Advanced Reproductive Center of Hawaii – FDA Inspection, Aug 10, 2018

Record Details

This FDA Inspection record concerns Christopher T.F. Huang M.D., Inc. dba Advanced Reproductive Center of Hawaii, with an inspection on August 10, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.

Company
Christopher T.F. Huang M.D., Inc. dba Advanced Reproductive Center of Hawaii
Inspection Date
August 10, 2018
Product Type
Biologics
Office
Center for Biologics Evaluation and Research
Person
  • Tania Y. Hall
View Company Profile

ID · 5b4c0f64-50da-46f2-998a-bc3580f98e9b

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1062085
FDA center
Biologics
Project area
Blood and Blood Products
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 1271.75(a)(1)Risk factors, clinical evidence
  2. 21 CFR 1271.85(a)Infection with communicable disease agents

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Christopher T.F. Huang M.D., Inc. dba Advanced Reproductive Center of Hawaii

5
DateClassificationOfficeProject area
March 27, 2025Not classifiedSan Francisco District Office
April 28, 2023NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
December 3, 2015NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
June 7, 2013NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
August 10, 2009NAICenter for Biologics Evaluation and ResearchHuman Cellular, Tissue, and Gene Therapies
Other documents for Christopher T.F. Huang M.D., Inc. dba Advanced Reproductive Center of Hawaii
  • FDA Inspection 1265628 - 2025-03-27
  • FDA Inspection 1203902 - 2023-04-28
  • FDA Inspection 951149 - 2015-12-03
  • FDA Inspection 835168 - 2013-06-07
  • FDA Inspection 613088 - 2009-08-10

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