FDA inspection
Blaine Labs Inc: FDA inspection ending Sep 30, 2019
FDA inspection 1103359 · Official Action Indicated (OAI) · Santa Fe Springs, CA
Key facts
| Inspection ID | 1103359 |
|---|---|
| Firm | Blaine Labs Inc |
| FEI number | 3001744192 |
| Address | 11037 Lockport Pl |
| City | Santa Fe Springs |
| State | CA |
| ZIP | 90670-4634 |
| Fiscal year | 2019 |
| Inspection end date | Sep 30, 2019 |
| Classification | Official Action Indicated (OAI) |
| Project area | Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|Drug Quality Assurance|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug 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Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation|OTC Drug Evaluation|Over-the-Counter Drug Evaluation |
| Product type | Drugs |
| Warning letter | 598733 |
At a glance
- 10–99 Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data