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FDA Inspection
•Cosmed of New Jersey•October 28, 2014

FDA Inspection 902142 - Cosmed of New Jersey - October 28, 2014

Record Details

This FDA Inspection record concerns Cosmed of New Jersey, with an inspection on October 28, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company
Cosmed of New Jersey
Inspection Date
October 28, 2014
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 8a90f35f-7205-4f02-924d-6e1c4b57bbf0

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
902142
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

FDA Citations

1
  1. 21 CFR 820.100(a)Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Cosmed of New Jersey

5
DateClassificationOfficeProject area
April 24, 2026Not classifiedNew Jersey District OfficeCompliance: Devices
June 8, 2023VAICenter for Devices and Radiological HealthCompliance: Devices
December 19, 2019NAICenter for Devices and Radiological HealthCompliance: Devices
April 20, 2017VAICenter for Devices and Radiological HealthBioresearch Monitoring
August 18, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Cosmed of New Jersey
  • FDA Inspection 1313802 - 2026-04-24
  • FDA Inspection 1208476 - 2023-06-08
  • FDA Inspection 1123230 - 2019-12-19
  • FDA Inspection 1011474 - 2017-04-20
  • FDA Inspection 740406 - 2011-08-18

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