PPD Development, L.P.

FDA Regulatory Profile

PPD Development, L.P. has 0 FDA recalls, 18 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "PPD Development, L.P." and its spelling variants "Ppd Development, L.P", "Ppd Development".

Latest inspection
May 1, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections18Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA Record by Year

PPD Development, L.P.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

PPD Development, L.P.: FDA inspections per year 2017: 0 inspections020172018: 3 inspections320182019: 4 inspections420192020: 0 inspections020202021: 1 inspections120212022: 1 inspections120222023: 0 inspections020232024: 0 inspections020242025: 1 inspections120252026: 2 inspections22026
YearInspectionsOAIWarning lettersRecall recordsClass I
202620000
202510000
202400000
202300000
202210000
202110000
202000000
201940000
201830000
201700000

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.

Recent FDA Inspections

18 inspections from Jan 23, 2009 to May 1, 2026.

DateSiteProductClassificationFEI
May 1, 2026Middleton, WIBiologicsNo Action Indicated (NAI)2129896
Apr 22, 2026Richmond, VADrugsNo Action Indicated (NAI)1121680
Sep 25, 2025Middleton, WIDrugsVoluntary Action Indicated (VAI)2129896
Oct 7, 2022Las Vegas, NVDrugsNo Action Indicated (NAI)3013505268
Jul 16, 2021Middleton, WIBiologicsVoluntary Action Indicated (VAI)2129896
Nov 18, 2019Richmond, VADrugsNo Action Indicated (NAI)1121680
Sep 19, 2019Middleton, WIDrugsNo Action Indicated (NAI)2129896
Apr 26, 2019Middleton, WIDrugsNo Action Indicated (NAI)3004105214
Mar 22, 2019Richmond, VADrugsNo Action Indicated (NAI)1121680
Nov 2, 2018Austin, TXDrugsNo Action Indicated (NAI)3011410938
May 18, 2018Middleton, WIDrugsVoluntary Action Indicated (VAI)2129896
Apr 12, 2018Richmond, VADrugsVoluntary Action Indicated (VAI)1121680
Jan 15, 2015Morrisville, NCDrugsNo Action Indicated (NAI)3003974035
Nov 20, 2013Middleton, WIDrugsNo Action Indicated (NAI)2129896
Mar 16, 2012Morrisville, NCDrugsNo Action Indicated (NAI)3003974035
Nov 9, 2011Middleton, WIDrugsNo Action Indicated (NAI)2129896
Jul 24, 2009Middleton, WIDrugsNo Action Indicated (NAI)2129896
Jan 23, 2009Morrisville, NCDrugsNo Action Indicated (NAI)3003974035

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.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-Inspected Facilities

6 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 2129896Middleton, WI8May 1, 2026
FEI 1121680Richmond, VA4Apr 22, 2026
FEI 3013505268Las Vegas, NV1Oct 7, 2022
FEI 3004105214Middleton, WI1Apr 26, 2019
FEI 3011410938Austin, TX1Nov 2, 2018
FEI 3003974035Morrisville, NC3Jan 15, 2015

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