FDA Inspection
Alliance Medical Products, Inc. DBA Siegfried CompanyAlliance Medical Products, Inc. DBA Siegfried Company – FDA Inspection, May 26, 2017
Record Details
This FDA Inspection record concerns Alliance Medical Products, Inc. DBA Siegfried Company, with an inspection on May 26, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- May 26, 2017
- Product Type
- Drugs
- People
- Amanda L. Fyles (Company Rep)
- Evelyn W. Ladines (Issuing Officer)
- Linda Thai (FDA Associated Person)
- Yasamin Ameri (FDA Associated Person)
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ID · e5369e63-7fa0-42f0-8049-aae157d51094
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1019222
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
10- 21 CFR 211.160(a)Following/documenting laboratory controls
- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.165(e)Test methods
- 21 CFR 211.165(f)Failing drug products not rejected
- 21 CFR 211.192Written record of investigation incomplete
- 21 CFR 211.22(d)Procedures not in writing, fully followed
- 21 CFR 211.25(a)Training , Education , Experience overall
- 21 CFR 211.42(c)(3)Released Material Area
- 21 CFR 211.68(a)Calibration/Inspection/Checking not done
- 21 CFR 211.68(b)input/output verification
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Other FDA inspections of Alliance Medical Products, Inc. DBA Siegfried Company
13| Date | Classification | Office | Project area |
|---|---|---|---|
| November 7, 2025 | VAI | Los Angeles District Office | Drug Quality Assurance |
| May 5, 2023 | Not classified | Los Angeles District Office | |
| May 21, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 14, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| August 21, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Alliance Medical Products, Inc. DBA Siegfried Company
- FDA Inspection 1286002 - 2025-11-07
- FDA Inspection 1206645 - 2023-05-05
- FDA Inspection 1142420 - 2021-05-21
- FDA Inspection 1084040 - 2019-02-14
- FDA Inspection 939504 - 2015-08-21
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