FDA Inspection
Altaire Pharmaceuticals, Inc.Altaire Pharmaceuticals, Inc. – FDA Inspection, Nov 19, 2010
Record Details
This FDA Inspection record concerns Altaire Pharmaceuticals, Inc., with an inspection on November 19, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- November 19, 2010
- Product Type
- Drugs
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ID · 1d8c10b7-6a12-4bd7-80a2-fdfb34bac157
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 704834
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
12- 21 CFR 211.188Prepared for each batch, include complete information
- 21 CFR 211.56(a)Sanitation--buildings not clean, free of infestation
- 21 CFR 211.58Buildings not maintained in good state of repair
- 21 CFR 211.46(b)Equipment for Environmental Control
- 21 CFR 211.130(d)Examination of packaging and labeling
- 21 CFR 211.130(b)Unlabeled filled containers controls
- 21 CFR 211.130(e)Packaging line inspection before use
- 21 CFR 211.113(a)Procedures for non-sterile drug products
- 21 CFR 211.28(a)Protective Apparel Not Worn
- 21 CFR 211.110(d)Rejected in-process materials not quarantined
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Other FDA inspections of Altaire Pharmaceuticals, Inc.
13| Date | Classification | Office | Project area |
|---|---|---|---|
| April 21, 2026 | Not classified | New York District Office | Drug Quality Assurance |
| October 21, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| February 11, 2022 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 19, 2019 | OAI | Center for Veterinary Medicine | Generic Drug Evaluation |
| March 9, 2017 | VAI | Center for Veterinary Medicine | Monitoring of Marketed Animal Drugs, Feed, and Devices |
Other documents for Altaire Pharmaceuticals, Inc.
- FDA Inspection 1314330 - 2026-04-21
- FDA Inspection 1251507 - 2024-10-21
- FDA Inspection 1162640 - 2022-02-11
- FDA Inspection 1089315 - 2019-04-19
- FDA Inspection 1005208 - 2017-03-09
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