Information Collection
Reporting: Adverse Drug Experience & Product / Manufacturing Defects Voluntary reporting Using Form FDa 1932a
IC 197279 under ICR 201412-0910-009 · OMB 0910-0284.
⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0284 can be found here:
Documents and Forms
| Document Name | Document Type |
|---|---|
Reporting: Adverse Drug Experience & Product / Manufacturing Defects Voluntary reporting Using Form FDa 1932a |
Form and Instruction |
Form FDA 1932a.pdf | Form and Instruction |