FDA applicant

Investigacion Farmaceutica S.A. DE C.V.

Mexico, MX24 decisions1989–19890 recalls

FDA records 24 decisions for Investigacion Farmaceutica S.A. DE C.V. (Mexico, MX) in 1989: 24 510(k) clearances. Most are in product codes JTN (Susceptibility Test Discs, Antimicrobial) and GHC (Tube, Sedimentation Rate). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, microbiology panel, where it files most

How often FDA has decided Investigacion Farmaceutica S.A. DE C.V.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Investigacion Farmaceutica S.A. DE C.V. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Investigacion Farmaceutica S.A. DE C.V. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Investigacion Farmaceutica S.A. DE C.V.

Which product codes does it file in?

What has FDA decided for it lately?