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FDA Inspection
•Pillar5 Pharma Inc.•February 6, 2015

Pillar5 Pharma Inc. – FDA Inspection, Feb 6, 2015

Record Details

This FDA Inspection record concerns Pillar5 Pharma Inc., with an inspection on February 6, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Pillar5 Pharma Inc.
Inspection Date
February 6, 2015
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · e4104669-72d1-459a-98e2-ca038ce3404e

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
917128
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

4
  1. 21 CFR 211.25(a)Training--operations, GMPs, written procedures
  2. 21 CFR 211.68(a)Written calibration / inspection records not kept
  3. 21 CFR 211.166(a)Results not used for expiration dates, storage cond.
  4. 21 CFR 211.166(a)Written program not followed

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Pillar5 Pharma Inc.

9
DateClassificationOfficeProject area
June 5, 2026Not classifiedOffice of Inspections and InvestigationsDrug Quality Assurance
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
View all 9 other inspections on the company page
Other documents for Pillar5 Pharma Inc.
  • FDA Inspection 1323174 - 2026-06-05
  • FDA Inspection 1261773 - 2025-02-07
  • FDA Inspection 1226692 - 2023-12-15
  • FDA Inspection 1119040 - 2020-02-21
  • FDA Inspection 1058599 - 2018-05-17

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