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FDA Inspection
•Malladi Drugs & Pharmaceuticals Ltd.•August 4, 2017

Malladi Drugs & Pharmaceuticals Ltd. – FDA Inspection, Aug 4, 2017

Record Details

This FDA Inspection record concerns Malladi Drugs & Pharmaceuticals Ltd., with an inspection on August 4, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Malladi Drugs & Pharmaceuticals Ltd.
Inspection Date
August 4, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Saleem A. Akhtar
View Company Profile

ID · 4fa99313-3ee2-4876-bc4d-03a16fca7105

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1022300
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Malladi Drugs & Pharmaceuticals Ltd.

4
DateClassificationOfficeProject area
July 3, 2026Not classifiedOffice of Inspections and Investigations
January 31, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 9, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 19, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Malladi Drugs & Pharmaceuticals Ltd.
  • FDA Inspection 1331272 - 2026-07-03
  • FDA Inspection 1119575 - 2020-01-31
  • FDA Inspection 1070896 - 2018-10-09
  • FDA Inspection 910002 - 2014-12-19

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