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FDA Inspection
•Anqiu Lu'an Pharmaceutical Co., Ltd.•May 18, 2018

Anqiu Lu'an Pharmaceutical Co., Ltd. – FDA Inspection, May 18, 2018

Record Details

This FDA Inspection record concerns Anqiu Lu'an Pharmaceutical Co., Ltd., with an inspection on May 18, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Anqiu Lu'an Pharmaceutical Co., Ltd.
Inspection Date
May 18, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Saleem A. Akhtar
View Company Profile

ID · 2e868e44-b7d5-4ee9-aa21-1cf61026f374

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1054214
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Anqiu Lu'an Pharmaceutical Co., Ltd.

5
DateClassificationOfficeProject area
September 26, 2025Not classifiedOffice of Inspections and Investigations
April 1, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 20, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 1, 2011NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 1, 2009VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Anqiu Lu'an Pharmaceutical Co., Ltd.
  • FDA Inspection 1287724 - 2025-09-26
  • FDA Inspection 969509 - 2016-04-01
  • FDA Inspection 850473 - 2013-09-20
  • FDA Inspection 733757 - 2011-07-01
  • FDA Inspection 632221 - 2009-10-01

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