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FDA Inspection
•J.M. Murray Center, Inc.•September 19, 2025

J.M. Murray Center, Inc. – FDA Inspection, Sep 19, 2025

Record Details

This FDA Inspection record concerns J.M. Murray Center, Inc., with an inspection on September 19, 2025, issued by the New York District Office, covering human drugs.

Company
J.M. Murray Center, Inc.
Inspection Date
September 19, 2025
Product Type
Human Drugs
Office
New York District Office
Person
  • John D. McIntosh (Issuing Officer)
View Company Profile

ID · 0908d792-43f3-4a92-b613-f4b084b2adcf

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1282356
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

4
  1. 21 CFR 211.67(b)(3)Cleaning SOPs/instructions
  2. 21 CFR 211.180(e)Records reviewed annually
  3. 21 CFR 211.166(a)Lack of written stability program
  4. 21 CFR 211.100(a)Absence of Written Procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of J.M. Murray Center, Inc.

6
DateClassificationOfficeProject area
April 30, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 17, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 21, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 13, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 26, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for J.M. Murray Center, Inc.
  • FDA Inspection 1140968 - 2021-04-30
  • FDA Inspection 983258 - 2016-08-17
  • FDA Inspection 846924 - 2013-08-21
  • FDA Inspection 799540 - 2012-09-13
  • FDA Inspection 727609 - 2011-05-26

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