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FDA 483表
FDA調查人員在設施檢查結束時出具的檢查觀察表。483表列出可能構成FD&C法違規的情況。企業必須在15個工作日內回應。
Last reviewed 2026-08-05 · Reviewed by MedFlux Editorial Board · Editorial policy
Expanded process notes below are currently maintained in English; the short definition above is localized. See our editorial policy.
WHEN IT APPLIES
FDA Form 483 lists inspectional observations when investigators observe conditions that may violate the FD&C Act and related regulations.
PROCESS / STEPS
- Receive and review observations promptly.
- Investigate root causes; prepare a thorough written response.
- Implement CAPA with effectiveness checks.
- Track to inspection classification outcomes (e.g., VAI/OAI).
EXAMPLES
- Incomplete CAPA responses to 483 observations can escalate to warning letters.
RELATED GUIDES & TOOLS
SOURCES
Track regulatory signals related to FDA 483表 across 27 authorities in real time.
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