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FDA Inspection
•Laboratoires Synth-Innove•February 10, 2017

Laboratoires Synth-Innove – FDA Inspection, Feb 10, 2017

Record Details

This FDA Inspection record concerns Laboratoires Synth-Innove, with an inspection on February 10, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Laboratoires Synth-Innove
Inspection Date
February 10, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Michael L. Casner (Company Rep)
View Company Profile

ID · 2aeddd00-4459-4403-8c99-8734697b48e4

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1004168
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Laboratoires Synth-Innove

1
DateClassificationOfficeProject area
October 28, 2009NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Laboratoires Synth-Innove
  • FDA Inspection 635167 - 2009-10-28

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