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FDA Inspection
•Murty Pharmaceuticals, Inc•March 28, 2025

Murty Pharmaceuticals, Inc – FDA Inspection, Mar 28, 2025

Record Details

This FDA Inspection record concerns Murty Pharmaceuticals, Inc, with an inspection on March 28, 2025, issued by the Cincinnati District Office, covering human drugs.

Company
Murty Pharmaceuticals, Inc
Inspection Date
March 28, 2025
Product Type
Human Drugs
Office
Cincinnati District Office
People
  • Geoffrey K. Kilili (Company Rep)
  • Heather R. Campbell (Issuing Officer)
View Company Profile

ID · 2b083c05-1eac-4b54-8466-47d2b64e2225

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1265169
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued, view the record

FDA Citations

2
  1. 21 CFR 211.182Specific information required in individual logs
  2. 21 CFR 211.160(b)Scientifically sound laboratory controls

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Murty Pharmaceuticals, Inc

5
DateClassificationOfficeProject area
April 17, 2019Not classifiedCincinnati District Office
January 14, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 15, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 22, 2011NAICenter for Drug Evaluation and ResearchBioresearch Monitoring
September 14, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Murty Pharmaceuticals, Inc
  • FDA Inspection 1087619 - 2019-04-17
  • FDA Inspection 1077569 - 2019-01-14
  • FDA Inspection 858433 - 2013-11-15
  • FDA Inspection 732158 - 2011-06-22
  • FDA Inspection 680956 - 2010-09-14

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