FEI establishment
Kerma Medical Products, Inc
FDA establishment FEI 1000123280 · Suffolk, United States
Key facts
| FEI number | 1000123280 |
|---|---|
| Legal name | Kerma Medical Products, Inc |
| City | Suffolk |
| Country | United States |
| Product types | Devices |
| Last inspection | Jul 7, 2017 |
At a glance
- 1–9 FDA inspections
- 1–9 No Action Indicated (NAI)
- 1–9 Voluntary Action Indicated (VAI)
- None Official Action Indicated (OAI)
- 1–9 Inspections with a Form 483
- 1–9 Citations
- 1–9 Repeat citations
- None Warning letters
- 1–9 Linked 510(k)s
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA establishments (FEI)
An FEI (FDA Establishment Identifier) is the number the FDA assigns to a site it inspects. FEIs of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection and compliance data