FDA inspection
Meridianmade Allerton, LLC: FDA inspection ending Apr 3, 2019
FDA inspection 1094149 · No Action Indicated (NAI) · Allerton, IA
Key facts
| Inspection ID | 1094149 |
|---|---|
| Firm | Meridianmade Allerton, LLC |
| FEI number | 1921383 |
| Address | 211 N Central Ave |
| City | Allerton |
| State | IA |
| ZIP | 50008 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Apr 3, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Foodborne Biological Hazards |
| Product type | Food/Cosmetics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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