Home / Companies / G.D. Searle And Co.

G.D. Searle And Co.

FDA Regulatory Profile

G.D. Searle And Co. has 0 FDA recalls, 1 inspection, 56 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "G.D. Searle And Co." and its spelling variants "G.D. Searle And", "G.D. Searle".

Latest inspection
Dec 20, 2017 · NAI
Latest 510(k)
May 25, 1982

Reviewing G.D. Searle And Co. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check G.D. Searle And Co. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances56Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA inspections

1 inspection on Dec 20, 2017.

DateSiteProductClassificationFEI
Dec 20, 2017New York, NYDrugsNo Action Indicated (NAI)3013953150
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3013953150New York, NY1Dec 20, 2017

Recent 510(k) clearances

56 510(k) clearances from Jul 19, 1976 to May 25, 1982. Showing the 20 most recent. View all 56 510(k) clearances

K-NumberDeviceDate
K821159IN-LINE OXYGEN MONITORING SYSTEMMay 25, 1982
K811068BYPASS COILMay 27, 1981
K811071VENOUS OXYGEN PROBEMay 5, 1981
K803238INTRAVASCULAR CATHETERApr 23, 1981
K810630SILICONE ELASTOMER COATED LATEX FOLEYMar 31, 1981
K810131ADMINISTRATION SETFeb 26, 1981
K802485SEARLE VASCULAR LOOPSFeb 12, 1981
K801805METRONIDAZOLE DISCSFeb 10, 1981
K810112SWR DISPOSABLE PREP RAZORFeb 4, 1981
K802213WHITE KNIGHT BOVIE CORD/SUCTION TUBEOct 10, 1980
K802280WHITE KNIGHT DRAPE SEALOct 10, 1980
K801415LATEX FOLEY CATHETER (HYDROMER COATED)Aug 20, 1980
K801414ERYTHROCATH INTRAVENOUS CATHETER PLA. U.Aug 13, 1980
K800815ENTERAL & NASOGASTRIC SOL. ADMIN. SETJul 21, 1980
K800928WHITE KNIGHT SUPPLEMENTAL DRAPEMay 20, 1980
K800927WHITE KNIGHT DISP. STERILE BACK GOWNMay 20, 1980
K800929WHITE KNIGHT SURGICAL PACKMay 20, 1980
K800609CATHETER STYLETApr 10, 1980
K800611BOUGIE A BOULEApr 8, 1980
K800607SUPRAPUBIC TROCARApr 8, 1980

Need more than this page shows? Ask about G.D. Searle And Co. in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.

Get a free API key

Prefer a PDF? Request a free supplier snapshot.

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.