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FDA Inspection
•SkyePharma Production SAS•May 31, 2013

SkyePharma Production SAS – FDA Inspection, May 31, 2013

Record Details

This FDA Inspection record concerns SkyePharma Production SAS, with an inspection on May 31, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
SkyePharma Production SAS
Inspection Date
May 31, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · cc0dde1d-85bd-495c-9da0-5f946ecac2d6

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
838912
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of SkyePharma Production SAS

5
DateClassificationOfficeProject area
October 27, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 7, 2023Not classifiedOffice of Inspections and Investigations
September 6, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 19, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 2, 2010VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for SkyePharma Production SAS
  • FDA Inspection 1265624 - 2023-10-27
  • FDA Inspection 1205869 - 2023-04-07
  • FDA Inspection 1105498 - 2019-09-06
  • FDA Inspection 938881 - 2015-06-19
  • FDA Inspection 659061 - 2010-04-02

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