FDA Inspection
Sciegen Pharmaceuticals IncSciegen Pharmaceuticals Inc – FDA Inspection, Jan 9, 2015
Record Details
This FDA Inspection record concerns Sciegen Pharmaceuticals Inc, with an inspection on January 9, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Sciegen Pharmaceuticals Inc
- Inspection Date
- January 9, 2015
- Product Type
- Drugs
View Company Profile
ID · ae103174-e954-404b-99f7-cc845da80edb
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 911142
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
1- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of Sciegen Pharmaceuticals Inc
13| Date | Classification | Office | Project area |
|---|---|---|---|
| May 15, 2026 | Not classified | New York District Office | Drug Quality Assurance |
| December 19, 2025 | NAI | Bioresearch Monitoring | |
| February 20, 2024 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 21, 2023 | OAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| September 2, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Sciegen Pharmaceuticals Inc
- FDA Inspection 1317246 - 2026-05-15
- FDA Inspection 1297968 - 2025-12-19
- FDA Inspection 1229682 - 2024-02-20
- FDA Inspection 1204858 - 2023-04-21
- FDA Inspection 1178870 - 2022-09-02
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