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FDA Inspection
•Watson Laboratories Inc•April 21, 2014

Watson Laboratories Inc – FDA Inspection, Apr 21, 2014

Record Details

This FDA Inspection record concerns Watson Laboratories Inc, with an inspection on April 21, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Watson Laboratories Inc
Inspection Date
April 21, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · ccf6449c-f977-4d75-87b0-c6ddd1dc67ff

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
875552
FDA center
Human Drugs
Project area
Drug Quality Assurance

FDA Citations

3
  1. 21 CFR 211.160(b)Scientifically sound laboratory controls
  2. 21 CFR 211.165(e)Test methods
  3. 21 CFR 211.192Investigations of discrepancies, failures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Watson Laboratories Inc

6
DateClassificationOfficeProject area
January 30, 2017NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 8, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 26, 2012OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 13, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
August 16, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Watson Laboratories Inc
  • FDA Inspection 1001328 - 2017-01-30
  • FDA Inspection 907020 - 2014-12-08
  • FDA Inspection 802315 - 2012-11-26
  • FDA Inspection 756889 - 2011-12-13
  • FDA Inspection 676262 - 2010-08-16

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