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FDA Inspection
•Cosmed of New Jersey•April 20, 2017

FDA Inspection 1011474 - Cosmed of New Jersey - April 20, 2017

Record Details

This FDA Inspection record concerns Cosmed of New Jersey, with an inspection on April 20, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company
Cosmed of New Jersey
Inspection Date
April 20, 2017
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 85041c86-e10b-433d-a0b1-eb2e3ba344fd

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1011474
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices

FDA Citations

2
  1. 21 CFR 820.25(b)Training records
  2. 21 CFR 820.70(g)Equipment Installation, Placement, Specified Requirements

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
October 28, 2014VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
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 902142 - 2014-10-28
  • FDA Inspection 740406 - 2011-08-18

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