FDA issued a Warning Letter to Diopsys, Inc. on 2/1/2005 for a previous inspection.
483 Diopsys Mar 2010

483 Diopsys Mar 2010

Frank Marciniak FDA$119.00 - Available Now

FDA investigators audited the Diopsys - Pine Brook, NJ, United States facility and issued inspectional observations (via FDA 483) on 01 Mar 2010.

Product details

  • Category: Medical Devices & Rad Health
  • Inspection end: 01 Mar 2010
  • Location: Pine Brook, United States
  • FEI: 3004174467
Add To Cart