FDA Inspection
Carie Boyd Pharmaceuticals LLCCarie Boyd Pharmaceuticals LLC – FDA Inspection, Jul 18, 2025
Record Details
This FDA Inspection record concerns Carie Boyd Pharmaceuticals LLC, with an inspection on July 18, 2025, issued by the Dallas District Office, covering human drugs.
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ID · 095b4bfe-cd8e-4e95-8485-7617c840de0f
Inspection Facts
- Inspection number
- 1275006
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
5- 21 CFR 211.110(a)Written in-process control procedures
- 21 CFR 211.113(b)Procedures for sterile drug products
- 21 CFR 211.188(b)Batch production and Batch Control Record Requirements
- 21 CFR 211.192Investigations of discrepancies, failures
- 21 CFR 211.63Equipment Design, Size and Location
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Other FDA inspections of Carie Boyd Pharmaceuticals LLC
6| Date | Classification | Office | Project area |
|---|---|---|---|
| September 8, 2026 | Not classified | Dallas District Office | Drug Quality Assurance |
| June 21, 2024 | OAI | Drug Quality Assurance | |
| June 27, 2022 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 12, 2019 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 12, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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