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FDA Inspection
•Pharmachemie B.V. dba Teva Pharmachemie•June 28, 2013

Pharmachemie B.V. dba Teva Pharmachemie – FDA Inspection, Jun 28, 2013

Record Details

This FDA Inspection record concerns Pharmachemie B.V. dba Teva Pharmachemie, with an inspection on June 28, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Pharmachemie B.V. dba Teva Pharmachemie
Inspection Date
June 28, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 218a1564-f80e-4501-a70b-a796075d2685

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
843559
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

1
  1. 21 CFR 211.100(a)Absence of Written Procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Pharmachemie B.V. dba Teva Pharmachemie

6
DateClassificationOfficeProject area
October 17, 2024VAIDrug Quality Assurance
September 9, 2021NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 17, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 6, 2016Not classifiedOffice of Inspections and Investigations
May 29, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Pharmachemie B.V. dba Teva Pharmachemie
  • FDA Inspection 1306540 - 2024-10-17
  • FDA Inspection 1240527 - 2021-09-09
  • FDA Inspection 1092106 - 2019-05-17
  • FDA Inspection 1000598 - 2016-12-06
  • FDA Inspection 941457 - 2015-05-29

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