FDA inspection
Calmo Manufacturing, Inc: FDA inspection ending Aug 4, 2023
FDA inspection 1213059 · No Action Indicated (NAI) · Huntington Beach, CA
Key facts
| Inspection ID | 1213059 |
|---|---|
| Firm | Calmo Manufacturing, Inc |
| FEI number | 3007621443 |
| Address | 16601 Burke Ln |
| City | Huntington Beach |
| State | CA |
| ZIP | 92647 |
| Country | United States |
| Fiscal year | 2023 |
| Inspection end date | Aug 4, 2023 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 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