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FDA Inspection
•Evans Manufacturing•October 11, 2018

Evans Manufacturing – FDA Inspection, Oct 11, 2018

Record Details

This FDA Inspection record concerns Evans Manufacturing, with an inspection on October 11, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company
Evans Manufacturing
Inspection Date
October 11, 2018
Product Type
Devices
Office
Center for Devices and Radiological Health
People
  • Juanita Banuelos (Company Rep)
  • Kevin N. Tran (Investigator)
View Company Profile

ID · 480f209b-014e-4263-91d7-a51a7a70b336

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1069494
FDA center
Medical Devices & Rad Health
Project area
Compliance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.198(a)Complaints
  2. 21 CFR 820.22Quality audits - Lack of or inadequate procedures

Full citation text and observation details available on the Dashboard.

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