FDA inspection
Gregory Manufacturing, Inc.: FDA inspection ending Sep 11, 2007
FDA inspection 488576 · No Action Indicated (NAI) · Holyoke, MA
Key facts
| Inspection ID | 488576 |
|---|---|
| Firm | Gregory Manufacturing, Inc. |
| FEI number | 1000120897 |
| Address | 102 Cabot St |
| City | Holyoke |
| State | MA |
| ZIP | 01040-5094 |
| Fiscal year | 2007 |
| Inspection end date | Sep 11, 2007 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes 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