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FDA Inspection
•Keystone Laboratories, Inc.•November 16, 2017

Keystone Laboratories, Inc. – FDA Inspection, Nov 16, 2017

Record Details

This FDA Inspection record concerns Keystone Laboratories, Inc., with an inspection on November 16, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Keystone Laboratories, Inc.
Inspection Date
November 16, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Marvin D. Jones (FDA Associated Person)
View Company Profile

ID · 66c5986b-40b7-4653-afb8-045f29b4dc17

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
1038087
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Keystone Laboratories, Inc.

7
DateClassificationOfficeProject area
February 5, 2016OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 13, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 12, 2014OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 15, 2013OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 29, 2012OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Keystone Laboratories, Inc.
  • FDA Inspection 984429 - 2016-02-05
  • FDA Inspection 917925 - 2015-03-13
  • FDA Inspection 897322 - 2014-09-12
  • FDA Inspection 846286 - 2013-08-15
  • FDA Inspection 798912 - 2012-08-29

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