FDA Inspection
Alliance Medical Products, Inc. DBA Siegfried CompanyAlliance Medical Products, Inc. DBA Siegfried Company – FDA Inspection, Nov 7, 2025
Record Details
This FDA Inspection record concerns Alliance Medical Products, Inc. DBA Siegfried Company, with an inspection on November 7, 2025, issued by the Los Angeles District Office, covering human drugs.
- Inspection Date
- November 7, 2025
- Product Type
- Human Drugs
View Company Profile
ID · a82fa971-a9ee-46c6-8a77-23cafd137604
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1286002
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.113(b)Validation lacking for sterile drug products
- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.192Extent of discrepancy, failure investigations
- 21 CFR 211.42(c)(10)(v)Cleaning System
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Alliance Medical Products, Inc. DBA Siegfried Company
13| Date | Classification | Office | Project area |
|---|---|---|---|
| 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 |
| May 26, 2017 | 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 1206645 - 2023-05-05
- FDA Inspection 1142420 - 2021-05-21
- FDA Inspection 1084040 - 2019-02-14
- FDA Inspection 1019222 - 2017-05-26
- FDA Inspection 939504 - 2015-08-21
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