FDA Device Establishments · JSON-LD · Markdown
FEI 3004945409 · Manufacture Device in the United States for Export Only · Status: Active
| FEI Number | 3004945409 |
|---|---|
| Owner / Operator | PFIZER INC. (#9924008) |
| Address | 400 Webro Road, Parsippany, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OUG |
| Regulation § (21 CFR) | 880.6310 |
| Proprietary names | MedCheck |
Source: openFDA. Public-domain (CC0).