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FDA Inspection
•Navajo Manufacturing Company•March 11, 2010

Navajo Manufacturing Company – FDA Inspection, Mar 11, 2010

Record Details

This FDA Inspection record concerns Navajo Manufacturing Company, with an inspection on March 11, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company
Navajo Manufacturing Company
Inspection Date
March 11, 2010
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · b2a0c296-1695-42bb-b231-bb452641dd7b

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
650990
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

FDA Citations

1
  1. 21 CFR 820.184DHR content

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Navajo Manufacturing Company

6
DateClassificationOfficeProject area
December 5, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
August 22, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 9, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 11, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 28, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Navajo Manufacturing Company
  • FDA Inspection 905874 - 2014-12-05
  • FDA Inspection 899142 - 2014-08-22
  • FDA Inspection 840309 - 2013-07-09
  • FDA Inspection 786600 - 2012-06-11
  • FDA Inspection 708089 - 2011-01-28

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