483 ReShape Lifesciences Dec 2017

483 ReShape Lifesciences Dec 2017

Susan Matthias FDA$119.00 - Available Now

FDA investigators audited the ReShape Lifesciences - Saint Paul, MN, United States facility and issued inspectional observations (via FDA 483) on 18 Dec 2017.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 18 Dec 2017
  • Location: Saint Paul, United States
  • FEI: 3005025697
Add To Cart