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FDA Inspection
•Swiss American CDMO, LLC•July 27, 2009

Swiss American CDMO, LLC – FDA Inspection, Jul 27, 2009

Record Details

This FDA Inspection record concerns Swiss American CDMO, LLC, with an inspection on July 27, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company
Swiss American CDMO, LLC
Inspection Date
July 27, 2009
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · f468495a-3973-4296-ac59-e1ba86808b93

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
599251
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

Other FDA inspections of Swiss American CDMO, LLC

8
DateClassificationOfficeProject area
December 16, 2024NAIDallas District OfficePostmarket Assurance: Medical Devices
December 19, 2022NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
March 31, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 12, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 28, 2018VAICenter for Devices and Radiological HealthCompliance: Devices
View all 8 other inspections on the company page
Other documents for Swiss American CDMO, LLC
  • FDA Inspection 1251710 - 2024-12-16
  • FDA Inspection 1193281 - 2022-12-19
  • FDA Inspection 1165937 - 2022-03-31
  • FDA Inspection 1114623 - 2019-12-12
  • FDA Inspection 1067042 - 2018-09-28

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