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FDA Inspection
•PureTek Corporation•January 21, 2011

PureTek Corporation – FDA Inspection, Jan 21, 2011

Record Details

This FDA Inspection record concerns PureTek Corporation, with an inspection on January 21, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
PureTek Corporation
Inspection Date
January 21, 2011
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 6b12333c-8a2a-4a51-ac1e-1035fbb9f7cf

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
707043
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of PureTek Corporation

9
DateClassificationOfficeProject area
March 7, 2025VAILos Angeles District OfficeDrug Quality Assurance
January 30, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 15, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 27, 2015VAICenter for Drug Evaluation and ResearchUnapproved and Misbranded Drugs
March 18, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 9 other inspections on the company page
Other documents for PureTek Corporation
  • FDA Inspection 1262436 - 2025-03-07
  • FDA Inspection 1116761 - 2020-01-30
  • FDA Inspection 1034952 - 2017-12-15
  • FDA Inspection 949735 - 2015-10-27
  • FDA Inspection 919565 - 2015-03-18

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