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APOTHECARY PRODUCTS, LLC. FDA Inspection Record

FEI 2183416 · Inspections, Form 483s, warning letters and import refusals

APOTHECARY PRODUCTS, LLC. is an FDA-registered facility (FEI 2183416) located in BURNSVILLE, MN, US. RegDataLab tracks 6 FDA inspections at this facility.

What FDA found at this site

Latest inspection
May 9, 2023: No Action Indicated (NAI)
Inspections on record
6 (1 VAI, 5 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Recalls as the recalling firm
1, latest Mar 30, 2023

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
May 9, 2023No Action Indicated (NAI)No citations listed
Sep 3, 2019Voluntary Action Indicated (VAI)Lack of or inadequate receiving acceptance procedures (21 CFR 820.80(b))
Equipment control activity documentation (21 CFR 820.72(a))
Process control procedures, Lack of or inadequate procedures (21 CFR 820.70(a))
Feb 25, 2019No Action Indicated (NAI)No citations listed
May 5, 2016No Action Indicated (NAI)No citations listed
Aug 14, 2015No Action Indicated (NAI)No citations listed
Oct 8, 2009No Action Indicated (NAI)No citations listed

Recalls

Newest first. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
Mar 30, 2023Class IIZ-1702-2023Eye and Ear Dropper, Product Code 67082 and 1 more product
Potential for glass dropper to have glass particulate on the outside surface of the dropper bulb.

FDA record score

4 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 15, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

2 records behind this number
RecordDatePoints x age weightAdds
Class II recall Z-1702-2023, this FEI as the recalling firmMar 30, 20234 x 0.62.4
Inspection classified VAISep 3, 20196 x 0.251.5

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 15, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 15, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 15, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Apothecary Products, LLC
Location
BURNSVILLE, MN (US)
Source
device

FDA data resources

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