Electronics Manufacturing and UV Instruments Support

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Quality & ITAR

All EIT facilities are  ISO 9001, ISO 13485 (medical) and ITAR registered. 

EIT's facilities in Leesburg and Salem are AS 9100 (aerospace) registered

EIT's Danville and Salem facilites are also FDA registered.  

EIT incorporates several steps to make sure that we deliver products that meet customer requirements. These steps include:

  • Understanding of customer requirements prior to quoting or accepting an order
  • Holding an NPI (New Product Introduction) meeting within EIT to review the planned build process which also includes inspection and data collection points
  • Use of SPC data to augment the continuous improvement of processes and product
  • Use of our document control/engineering change notice (ECN) system
  • Generation of work & test instructions including pictorials
  • Using post build feedback obtained from our customers to improve our processes