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FDA Inspection
•Delpharm Huningue S.A.S.•December 15, 2011

Delpharm Huningue S.A.S. – FDA Inspection, Dec 15, 2011

Record Details

This FDA Inspection record concerns Delpharm Huningue S.A.S., with an inspection on December 15, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Delpharm Huningue S.A.S.
Inspection Date
December 15, 2011
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · ace67737-dd0c-4848-b8a2-76812494f0b4

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
765433
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

3
  1. 21 CFR 211.84(d)(2)Establish reliability of supplier"s C of A
  2. 21 CFR 211.113(a)Procedures for non-sterile drug products
  3. 21 CFR 211.68(a)Calibration/Inspection/Checking not done

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Delpharm Huningue S.A.S.

5
DateClassificationOfficeProject area
November 30, 2023VAIMonitoring of Marketed Animal Drugs, Feed, and Devices
August 8, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 22, 2018NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
September 23, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 19, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Delpharm Huningue S.A.S.
  • FDA Inspection 1262708 - 2023-11-30
  • FDA Inspection 1125617 - 2019-08-08
  • FDA Inspection 1060634 - 2018-06-22
  • FDA Inspection 988001 - 2016-09-23
  • FDA Inspection 913598 - 2014-12-19

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