EFE produced both LT 1938 Stock and special Isle of Wight Class 483 models. They were available in either Network Southeast livery or the 'Dinosaur' livery. They are unpowered static models, although a number of motorising options are available from Branchlines or Metromodels.

fda 483是美国食品药品监督管理局（fda）在对企业进行现场检查后，记录检查中发现的问题并发出的一份文件。 这份文件通常以清单形式列出不符合法规要求的具体观察项，并要求企业针对这些问题采取纠正措施并提交整改计划。

Find many great new & used options and get the best deals for EFE 99932 CL. 483 ISLAND LINE 1938 STOCK TUBE TRAIN LONDON UNDERGROUND BACHMANN at the best online prices at eBay! Free shipping for many products!

对于483： FDA检察官在检察（inspection）中，如有任何观察项（Observation），则会当场出具FDA 483表。 此处不要以为观察项（Observation）是建议项（suggestion/ opportunity for improvement）或者轻微不合格（minor nonconformity）。

Interior (left) and exterior (right) door open/close buttons retro-fitted to the BR Class 483 units. As well as cosmetic and structural work, significant electrical works were required both to replace dilapidated wiring, and to allow the trains to work from the line's third rail electrical supply.

医疗器械或者IVD制造商都不想收到来自美国食品药品监督管理局（FDA）的483表格或警告信。 FDA 483表格正式名称为“现场观察报告”，通常被简称为“483表格”。 如果美国食品药品监督管理局（FDA）现场调查员发现您的医疗器械质量体系存在缺陷或违反《食品、药品或化妆品法案》的情况，则其会在现场检查结束时出具483表格。 收到美国食品药品监督管理局483表格后该怎么办？ 现场检查员将会把最终的483号表格提交给他/她的主管；假如发现的问题确实很严重，或者您 …

FDA 483表格，也称现场观察报告(Inspectional Observation)， 它是FDA 检查官根据 cGMP 规范，对医药企业的质量体系进行现场检查过程中所发现的不符合cGMP 之处列出的总结清单。FDA483表格是一份报告，它并不包括检查时有疑问或未发现的缺陷情况。

Class 483 2-car EMU in Isle of Wight Island Line red and white livery - non-motorised dummy

OO Gauge (1:76 Scale) Class 483 2-car EMU 483 005 in Network SouthEast livery - non-motorised dummy. Thousands of products available to purchase from Rails of Sheffield. Shop Now. This model is not fitted with a motor. This will run on OO gauge track but is very poor running as it is not fitted with pin point axles.

FDA 483 报告（缺陷报告），也称现场观察报告（Inspectional Observation）， 它是FDA 检查官根据cGMP 规范，对医药企业的质量体系进行现场检查过程中所发现的不符合cGMP 之处列出的总结清单。