Following the rapid rise of organic metal halide perovskites towards commercial application in thin film solar cells, inorganic alternatives attracted great interest with their potential of longer device lifetime due to the stability improvement under elevated temperatures and moisture ingress. Among them, cesium lead iodide (CsPbI3) has gained significant attention due to similar electronic and optical properties to methylammonium lead iodide (MAPbI3), with a band gap of 1.7 eV, high absorption coefficient and large diffusion length, while also offering the advantage of being completely inorganic, providing a higher thermal stability and preventing material degradation. On a device level however, it seems also essential to replace organic transport layers by inorganic counterparts to further prevent degradation. In addition, devices are mostly fabricated by spin coating, limiting their reproducibility and scalability; in this case, exploring all-evaporated devices allows to improve the quality of the layers and to increase their reproducibility. In this work, we focus on the deposition of CsPbI3 by CsI and PbI2 co-evaporation. We fabricate devices with an allinorganic, all-evaporated structure, employing NiO and TiO2 as transport layers, and evaluate these devices for both photodetector and solar cell applications. As a photodetector, low leakage current, high EQE and detectivity, and fast rise and decay times were obtained; while as a solar cell, acceptable efficiencies were achieved. These all-inorganic, all-evaporated devices represent one step forward towards higher stability and reproducibility, while enabling large area-compatibility and easier integration with other circuitry and, in future, the possible commercialization of perovskite-based technology.