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FDA Inspection
•Laboratorios Zepol S.A.•March 29, 2017

Laboratorios Zepol S.A. – FDA Inspection, Mar 29, 2017

Record Details

This FDA Inspection record concerns Laboratorios Zepol S.A., with an inspection on March 29, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Laboratorios Zepol S.A.
Inspection Date
March 29, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Jose A. Cruz Gonzalez
View Company Profile

ID · 423bfe2d-e204-4f2a-8e92-01eacbe9c6a1

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1008927
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Laboratorios Zepol S.A.

2
DateClassificationOfficeProject area
November 17, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 9, 2023NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Laboratorios Zepol S.A.
  • FDA Inspection 1223082 - 2023-11-17
  • FDA Inspection 1204690 - 2023-03-09

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