Calibration of Solid-State Nuclear Track Detectors - SSNTD in the diffusion chamber in most cases assumes a constant radon concentration outside the diffusion chamber and a steady state. Although this has been proven to be a valid approximation in most cases, the fact is that the radon concentration outside the chamber is not constant. In this way, the detectors are calibrated to measure the mean radon concentration. For this reason, there is doubt if the time-dependent concentration in dwellings results in the same number of tracks on the detector as the time-averaged radon concentration for the same exposure period. To obtain an answer, time-dependent and steady-state diffusion equations for radon and its progeny were solved. Then the number of tracks on the detector was calculated for these two cases and compared. For that goal, software for solving the time-dependent diffusion equation for time-varying external radon concentration was developed. Results show that concentrations measured using a diffusion chamber are the real concentrations at the measuring site. However, it was also found that the validity of results is not a universal property, as shown in the current paper. In some cases, results can be wrong. For some extreme conditions when diffusion coefficients are disrupted calibration using stationary conditions model will lead to incorrect results of real measurements in experiments where ambiental concentration is time-varying.