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FDA Inspection
•Formosa Laboratories, Inc.•November 9, 2018

Formosa Laboratories, Inc. – FDA Inspection, Nov 9, 2018

Record Details

This FDA Inspection record concerns Formosa Laboratories, Inc., with an inspection on November 9, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Formosa Laboratories, Inc.
Inspection Date
November 9, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Qin Xu (FDA Associated Person)
View Company Profile

ID · dbe4c0c8-52b5-4aae-ac88-14577688296e

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1075251
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Formosa Laboratories, Inc.

6
DateClassificationOfficeProject area
July 25, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 11, 2022NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 1, 2017Not classifiedOffice of Inspections and Investigations
January 22, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 10, 2012NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Formosa Laboratories, Inc.
  • FDA Inspection 1245465 - 2024-07-25
  • FDA Inspection 1192918 - 2022-11-11
  • FDA Inspection 1038338 - 2017-12-01
  • FDA Inspection 913500 - 2015-01-22
  • FDA Inspection 786046 - 2012-05-10

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