The table that follows lists tasks like those required of the U.S. Food and Drug Administration (FDA) in carrying out its responsibilities to regulate drug laboratories, along with an importance weighting of each tasks and the estimated minimum number of staff hours required to accomplish the task fully.

j Task Import Hours 1 Laboratory quality control program 10 1500 2 Analytical protocol 1 100 3 Drug protocol 2 50 4 Quality assurance guidelines 5 55 5 Safety programs 10 135 6 Stability of testing 5 490 7 Calibration of equipment 4 2000 Total 4330 Unfortunately only 3600 of the 4330 total hours are available to execute all tasks. FDA management seeks an allocation of the 3600 hours that addresses the goal hours in the table on the basis of minimizing total importance of undersatisfaction.
Formulate a goal LP to determine the most appropriate allocation.