Pc Marketing, Inc. FDA Record

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

  • Latest inspection VAI · Mar 7, 2019
  • Last warning letter 2012
Inspections 2 1 OAI
Recalls 0 0 Class I
Warning letters 1 Latest Oct 10, 2012
510(k) clearances 1 Latest Apr 14, 2016

Pc Marketing, Inc. has 0 FDA recalls, 2 inspections, 1 510(k) clearance and 1 compliance action on record. FDA has issued 1 warning letter to Pc Marketing, Inc., the most recent on Oct 10, 2012.

What these totals cover: FDA records filed under the name "Pc Marketing, Inc." and its spelling variant "Pc Marketing".

Latest inspection
Mar 7, 2019 · VAI
Latest 510(k)
Apr 14, 2016

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) clearances1Nov 15, 2026File dated Nov 9, 2026Current
Inspections2Nov 15, 2026Newest record Nov 5, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Pc Marketing, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Pc Marketing, Inc.: FDA inspections per year

YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202500000
202400000
202300000
202200000
202100000
202000000
201910000
201800000
201711000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

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Pc Marketing, Inc. FDA Warning Letters

1 warning letter on Oct 10, 2012.

IssuedSubjectIssuing officeClose-out letter
Oct 10, 2012 · Record page

A warning letter is FDA's formal notice that a company has violated FDA requirements. Each date links to the letter on fda.gov where FDA has it online. Search the text of every letter with the FDA warning letter search.

Recent FDA inspections

2 inspections from Jan 19, 2017 to Mar 7, 2019.

DateSiteProductClassificationFEI
Mar 7, 2019Ridgefield, NJDevicesVoluntary Action Indicated (VAI)1000122259
Jan 19, 2017Ridgefield, NJDevicesOfficial Action Indicated (OAI)1000122259
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.

Compliance Actions

FDA's compliance actions data lists 1 compliance action under Pc Marketing, Inc.: warning letters, injunctions and seizures. None came from FDA's Center for Tobacco Products.

Most recent: Warning Letter, Oct 10, 2012.

The warning letters in this data are listed above, together with the letters FDA posts online; a letter found in both is shown once. Other actions are not listed on this page. Search them with the FDA warning letter search or browse all compliance actions.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 1000122259Ridgefield, NJ2Mar 7, 2019

Recent 510(k) clearances

1 510(k) clearance on Apr 14, 2016.

K-NumberDeviceDate
K152364uwe sun tanning beds/booths P90, iBED EVG, iSUN HP, SILVERBULLET SE, LOTUSApr 14, 2016

Pc Marketing, Inc. and the FDA: common questions

Has Pc Marketing, Inc. received an FDA warning letter?

Yes. FDA has issued 1 warning letter to Pc Marketing, Inc.. The most recent is dated Oct 10, 2012.

Has Pc Marketing, Inc. received an FDA Form 483?

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

When did the FDA last inspect Pc Marketing, Inc.?

The most recent FDA inspection on file ended Mar 7, 2019 at Ridgefield, NJ and was classified VAI. FDA has 2 inspections of Pc Marketing, Inc. on file, 1 of them classified OAI (official action indicated).

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