Medical Device Manufacturers:
Catheter Mfg. (Components are in the correct position after assembly)
Stent Mfg. (Looking for the position of the Stent referencing the marker bands on the catheter)
Medical Tube Assemblies (Tube insert depth and seal quality)
Syringe Mfg. (Looking at 5 degrees or more on the angle of the needle after it has been packaged)
Medical Devices that need to be 100% quality assurance after assembly
Surgical Tray Packaging (Verifying that all of the items are in the tray and haven't been damaged during packaging)
Pacemaker Mfg. (Correct placement of the internal components)
Porosity problems (In plastic molded parts for the medical device industry)

Pharmaceutical Manufacturing and Packaging:
Transdermal Packaging (Counting the number of transdermal patches and verifying that the instructions are in the carton after it has been closed)
Bottle filling (Check Levels of pharmaceutical liquids in bottles)
Placement of instructions (Verifying that instructions are in the pharmaceutical package after the package has been sealed)
Checking for damaged components (Verify that all components have not been damaged after packaging)
Blister Packaging (Counting pills, looking for broken pills)

Automotive:
Critical electronic assemblies for automotive (Solder quality, internal pin placement, wire placement, etc.)
Automotive head lights (Air pressure in the bulb, internal weld or solder quality, filament measurement)
Verifying components after assembly (Component placement)

Semiconductor:
BGA Quality (Voids, bridging, Alignment, Coplanarity, Size, roundness, etc.)
Bond Wire (Placement or damage)

Consumable goods:
Golf Balls (Inner core quality)
Bottle Fill levels (Confirming bottle fill levels)
Internal plastic molding issues (Checking for any internal porosity)

 The U.S. Food and Drug Administration (FDA) have responsibility for assuring manufacturers produce cabinet x-ray systems that do not pose a radiation safety hazard. For most electronic products that emit radiation, safety regulation is divided between FDA and state regulatory agencies. Typically, FDA regulates the manufacture of the products and the states regulate the use of the products. For further information on FDA regulations that apply to manufacturers of electronic products that emit radiation (such as a cabinet x-ray system) see the FDA web site (http://www.fda.gov/cdrh/comp/eprc.html).