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FDA Inspection
•Pillar5 Pharma Inc.•June 5, 2026

Pillar5 Pharma Inc. – FDA Inspection, Jun 5, 2026

Record Details

This FDA Inspection record concerns Pillar5 Pharma Inc., with an inspection on June 5, 2026, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Pillar5 Pharma Inc.
Inspection Date
June 5, 2026
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Taichun Qin (FDA Associated Person)
  • Youkeun Kim
View Company Profile

ID · 797a6a97-028e-475d-bd9f-5894cfb5abda

Inspection Facts

Inspection number
1323174
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

4
  1. 21 CFR 211.113(b)Procedures for sterile drug products
  2. 21 CFR 211.188Prepared for each batch, include complete information
  3. 21 CFR 211.192Investigations of discrepancies, failures
  4. 21 CFR 211.42(c)(10)(v)Cleaning System

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Pillar5 Pharma Inc.

9
DateClassificationOfficeProject area
February 7, 2025VAIOffice of Inspections and InvestigationsDrug Quality Assurance
December 15, 2023OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
February 21, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 17, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 26, 2018VAICenter for Veterinary MedicinePre-Approval Eval. of Animal Drugs and Food Additives
View all 9 other inspections on the company page
Other documents for Pillar5 Pharma Inc.
  • FDA Inspection 1261773 - 2025-02-07
  • FDA Inspection 1226692 - 2023-12-15
  • FDA Inspection 1119040 - 2020-02-21
  • FDA Inspection 1058599 - 2018-05-17
  • FDA Inspection 1038745 - 2018-01-26

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Contact
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