Microline Scientific FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

  • No warning letters matched by name
Inspections 0 0 OAI
Recalls 0 0 Class I
Warning letters 0 None on file
510(k) clearances 14 Latest May 31, 1984

Microline Scientific has 0 FDA recalls, 0 inspections, 14 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Microline Scientific" is on file.

What these totals cover: FDA records filed under the name "Microline Scientific".

Latest 510(k)
May 31, 1984

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 11, 2026 (checked Nov 15, 2026, unchanged)File dated Nov 10, 2026Current
510(k) clearances14Nov 15, 2026File dated Nov 9, 2026Current
Inspections0Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Reviewing Microline Scientific 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 Microline Scientific 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

Recent 510(k) clearances

14 510(k) clearances from May 14, 1984 to May 31, 1984.

K-NumberDeviceDate
K841842DIFFERENTIAL CULTURE MED. MACCONKEY AGARMay 31, 1984
K841845SELECTIVE CULTURE MED. COLUMBIA CNAMay 31, 1984
K841586CHOCOLATE AGARMay 31, 1984
K841843DIFFERENTIAL CULTURE MED. LEVINE EMBMay 31, 1984
K841844DIFFERENTIAL CULTURE MEDIUM-BIGGY AGARMay 31, 1984
K841841DIFFERENTIAL CULTURE MED. MANNITOL SALTMay 25, 1984
K841839SELECTIVE CULTURE MED. SELECTIVE STREPMay 25, 1984
K841840SELECTIVE CULTURE MED. PHENYLETHYL ALCOMay 25, 1984
K841838ENRICHED CULTURE MED. TRYPTIC SOY AGARMay 21, 1984
K841837ENRICHED CULTURE MED. FLUID THIOGLYC0May 21, 1984
K841835MULTIPURPOSE CULTURE MEDIUMMay 14, 1984
K841836SELECTIVE CULTURE MED. TRICHOMONASMay 14, 1984
K841833CULTURE MEDIUM FOR PATHOGENIC NEISSERMay 14, 1984
K841834CULTURE MEDIUM FOR ANTIMICROBIAL SUSCEPMay 14, 1984

Microline Scientific and the FDA: common questions

Has Microline Scientific received an FDA warning letter?

No FDA warning letter addressed to the name "Microline Scientific" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Microline Scientific received an FDA Form 483?

FDA has not published a Form 483 for "Microline Scientific" in its reading room. FDA publishes some Form 483s, not all of them.

Need more than this page shows? Ask about Microline Scientific 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.

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

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