The Biotech Source, Inc.

FDA Regulatory Profile

The Biotech Source, Inc. has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Apr 26, 2012 · NAI

Reviewing The Biotech Source, Inc. 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.

Request a free FDA snapshot

Or get The Biotech Source, Inc.'s full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site, in Claude, Cursor or ChatGPT.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances0Oct 4, 2026Not statedCurrent
Inspections2Oct 25, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Biotech
Same company group
0120—
Bio-Tech
Same company group
0200—
Biotech Dental Smilers
Same company group
0100—

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 26, 2012Windham, MEDevicesNo Action Indicated (NAI)1220706
Oct 14, 2008Windham, MEBiologicsNo Action Indicated (NAI)1220706

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.