FDA Inspection
Lawrence Morton, M.D.Lawrence Morton, M.D. – FDA Inspection, Dec 7, 2023
Record Details
This FDA Inspection record concerns Lawrence Morton, M.D., with an inspection on December 7, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 21d8dffc-de1f-4d44-a1cc-ebbdbdac8cd7
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1224848
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
- Outcome
- Form 483 issued
FDA Citations
4- 21 CFR 312.62(b)Case history records- inadequate or inadequate
- 21 CFR 312.64(b)Safety Reports - Non-Serious Events
- 21 CFR 312.62(b)Case history records- inadequate or inadequate
- 21 CFR 312.64(b)Safety Reports - Non-Serious Events
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