FDA inspection
Krispak Inc: FDA inspection ending Jun 6, 2019
FDA inspection 1092558 · Grand Rapids, MI
Key facts
| Inspection ID | 1092558 |
|---|---|
| Firm | Krispak Inc |
| FEI number | 3003073292 |
| Address | 3883 Swank Dr SE |
| City | Grand Rapids |
| State | MI |
| ZIP | 49512-3968 |
| Fiscal year | 2019 |
| Inspection end date | Jun 6, 2019 |
| Product type | Food/Cosmetics |
At a glance
- None Citations
- 1–9 Posted citations
- No 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