Standard Practice for Amusement Ride and Device Manufacturer Quality Assurance Program and Manufacturing Requirements

SCOPE
1.1 This practice establishes the minimum requirements for a quality assurance program and the manufacturing of amusement rides and devices (including major modifications).
1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

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Historical
Publication Date
31-Mar-2004
Current Stage
Ref Project

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ASTM F1193-04 - Standard Practice for Amusement Ride and Device Manufacturer Quality Assurance Program and Manufacturing Requirements
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NOTICE: This standard has either been superseded and replaced by a new version or withdrawn.
Please contact ASTM International (www.astm.org) for the latest information.
Designation:F1193–04
Standard Practice for
Amusement Ride and Device Manufacturer Quality
1
Assurance Program and Manufacturing Requirements
This standard is issued under the fixed designation F 1193; the number immediately following the designation indicates the year of
original adoption or, in the case of revision, the year of last revision. A number in parentheses indicates the year of last reapproval. A
superscript epsilon (ϵ) indicates an editorial change since the last revision or reapproval.
1. Scope 5.1.1 This procedure shall provide the purchasing agent
with all the information required to order appropriate material.
1.1 This practice establishes the minimum requirements for
5.1.2 A receiving procedure shall be in effect so that
a quality assurance program and the manufacturing of amuse-
incoming material and components are checked against the
ment rides and devices (including major modifications).
purchasing specifications.
1.2 This standard does not purport to address all of the
5.1.3 Aprocedure shall be in effect so that material in stock
safety concerns, if any, associated with its use. It is the
can be properly identified for future use.
responsibility of the user of this standard to establish appro-
5.1.4 Documentation on any material, process, or compo-
priate safety and health practices and determine the applica-
nents certified shall be filed for reference.
bility of regulatory limitations prior to use.
6. Manufacturing
2. Referenced Documents
2
6.1 Amusement ride and device components and systems
2.1 AWS Standards:
shall be manufactured and assembled in accordance with the
As applicable.
3
designer/engineer specified criteria.
2.2 ASME Standards:
6.2 Changes to the designer/engineer specified criteria shall
As applicable.
be documented and approved by the designer/engineer or a
3. Significance and Use qualified engineer before components, subassemblies, or sys-
tems are placed into use.
3.1 The purpose of this practice is to provide the minimum
manufacturing requirements for amusement rides and devices
7. Inspection
and to provide the minimum requirements for a written quality
7.1 A procedure shall be in effect so that appropriate
assurance program for an amusement ride or device manufac-
inspections are made on manufactured parts and subassem-
turer, or component supplier. This is not intended to include
blies, for conformance with the designer/engineer specified
suppliers of off-the-shelf components (for example, fasteners,
criteria.
electrical wire, etc.).
7.2 A procedure shall be in effect so that appropriate
4. Drawing Control Procedure
inspections are made on purchased components.
7.3 A procedure shall be in effect so that completed subas-
4.1 A procedure shall be in effect so that appropriate
semblies,orwherepractical,theassembledamusementridesor
manufacturing drawings, their engineering revisions, and re-
devices are inspected prior to delivery.
lated documents are utilized.
7.4 Nonconforming components shall be identified and
5. Material and Component Control Procedure
evaluated for disposition as follows:
7.4.1 The non-conforming component shall be scrapped or
5.1 A procedure shal
...

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