Complete Pharmacy And Medical Solutions, LLC.

FDA Regulatory Profile

Complete Pharmacy And Medical Solutions, LLC. has 6 FDA recalls (2 Class I), 2 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest recall
D-0237-2021 · Class II · Nov 20, 2020
Latest inspection
Jan 23, 2019 · OAI

Reviewing Complete Pharmacy And Medical Solutions, LLC. 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 Complete Pharmacy And Medical Solutions, LLC. 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

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls6 (2 Class I)Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections2Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
D-0237-2021Class IIHUMAN CHORIONIC GONADOTROPIN 1,250 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in…Nov 20, 2020
D-0234-2021Class IIHUMAN CHORIONIC GONADOTROPIN 11,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in…Nov 20, 2020
D-0235-2021Class IIHUMAN CHORIONIC GONADOTROPIN 6,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in…Nov 20, 2020
D-0236-2021Class IIHUMAN CHORIONIC GONADOTROPIN 5,000 IU per vial Aso contains Mannitol 9%, Sodium Phosphate 2% in…Nov 20, 2020
D-0918-2017Class IHuman Chorionic Gonadotropin, 15,000 IU per vial, lyophilized for injection, Rx only, Complete…Apr 2, 2016
D-0917-2017Class IHuman Chorionic Gonadotropin, 125 IU HCG, in 0.5 ml syringe, subcutaneous administration, Rx only…Dec 29, 2015

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 23, 2019Miami Lakes, FLDrugsOfficial Action Indicated (OAI)3010922197
Aug 12, 2014Miami Lakes, FLDrugsOfficial Action Indicated (OAI)3010922197

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.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3010922197Miami Lakes, FL2Jan 23, 2019

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