• Failure to ensure policies and procedures were implemented and followed to ensure instrument reprocessing equipment was properly sanitized.
  • Autoclave was leaking onto shelves below.
  • There was no documentation on when autoclave was maintained, no work to have leak checked or fixed, and no documentation on when spore growth (mold) testing was done.
  • Failed to ensure proficiency testing specimens were run in the same way as patient samples
  • Failed to maintain lab records.
  • Failed to ensure that the panoscreen controls for RH testing were labeled the date they were put to use.
Report 2013 Report 2019
DISCLAIMER: All of the inspection reports on this site were acquired through public records request to state departments of health and public records online.