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The Wave Processing FDA Inspection Record

FEI 2000035667 · Inspections, Form 483s, warning letters and import refusals

The Wave Processing is an FDA-inspected facility (FEI 2000035667) located in Wilmington, CA, US. RegDataLab tracks 7 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Apr 18, 2025: No Action Indicated (NAI)
Inspections on record
7 (1 OAI, 5 VAI, 1 NAI)
Last OAI inspection
Jul 16, 2009
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

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
Apr 18, 2025No Action Indicated (NAI)HACCP plan implementation (21 CFR 123.6(b))
Signed and dated (21 CFR 123.6(d))
May 24, 2021Voluntary Action Indicated (VAI)Training of employees and records (21 CFR 117.4)
Monitoring record review adequacy (21 CFR 123.8(a)(3)(i))
HACCP plan implementation (21 CFR 123.6(b))
Signed and dated (21 CFR 123.6(d))
Oct 4, 2017Voluntary Action Indicated (VAI)Sanitation monitoring (21 CFR 123.11(b))
HACCP plan implementation (21 CFR 123.6(b))
Corrective action plan (21 CFR 123.6(c)(5))
Aug 1, 2014Voluntary Action Indicated (VAI)No HACCP plan (21 CFR 123.6(b))
HACCP plan implementation (21 CFR 123.6(b))
Calibration - adequacy (21 CFR 123.8(a)(2)(ii))
Critical control points (21 CFR 123.6(c)(2))
and 2 more
May 2, 2011Voluntary Action Indicated (VAI)Sanitation monitoring (21 CFR 123.11(b))
Sanitation monitoring documentation (21 CFR 123.11(b))
Monitoring - adequacy (21 CFR 123.6(c)(4))
HACCP plan implementation (21 CFR 123.6(b))
and 2 more
Sep 23, 2010Voluntary Action Indicated (VAI)Sanitation monitoring (21 CFR 123.11(b))
Sanitation Records (21 CFR 123.11(c))
Monitoring - adequacy (21 CFR 123.6(c)(4))
Records entries - timing (21 CFR 123.9(a))
and 8 more
Jul 16, 2009Official Action Indicated (OAI)Precautions against contamination--micro, foreign substances (21 CFR 110.10(b)(9))
Sanitation monitoring (21 CFR 123.11(b))
Monitoring - adequacy (21 CFR 123.6(c)(4))
Ongoing verification - complaints, calibration records (21 CFR 123.8(a)(2))
and 8 more

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 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 14, 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
The Wave Processing
Location
Wilmington, CA (US)
Source
inspections

FDA data resources

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