U.S. Navy Medicine Readiness And Training Command Rota Spain FDA Record

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

U.S. Navy Medicine Readiness And Training Command Rota Spain has 0 FDA recalls, 8 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "U.S. Navy Medicine Readiness And Training Command Rota Spain" is on file.

What these totals cover: FDA records filed under the name "U.S. Navy Medicine Readiness And Training Command Rota Spain".

Latest inspection
Aug 7, 2025 · NAI

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
Inspections8Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

U.S. Navy Medicine Readiness And Training Command Rota Spain's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

U.S. Navy Medicine Readiness And Training Command Rota Spain: FDA inspections per year 2017: 1 inspections120172018: 0 inspections020182019: 1 inspections120192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 1 inspections120232024: 0 inspections020242025: 1 inspections120252026: 0 inspections02026
YearInspectionsOAIWarning lettersRecall recordsClass I
202600000
202510000
202400000
202310000
202200000
202100000
202000000
201910000
201800000
201710000

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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Recent FDA inspections

8 inspections from Jun 16, 2009 to Aug 7, 2025.

DateSiteProductClassificationFEI
Aug 7, 2025Rota, SpainBiologicsNo Action Indicated (NAI)3002809467
Jul 25, 2023Rota, SpainBiologicsNo Action Indicated (NAI)3002809467
May 14, 2019Rota, SpainBiologicsVoluntary Action Indicated (VAI)3002809467
May 17, 2017Rota, SpainBiologicsVoluntary Action Indicated (VAI)3002809467
Jun 1, 2015Rota, SpainBiologicsNo Action Indicated (NAI)3002809467
Jun 18, 2013Rota, SpainBiologicsNo Action Indicated (NAI)3002809467
Jun 23, 2011Rota, SpainBiologicsNo Action Indicated (NAI)3002809467
Jun 16, 2009Rota, SpainBiologicsNo Action Indicated (NAI)3002809467
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.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3002809467Rota, Spain8Aug 7, 2025

U.S. Navy Medicine Readiness And Training Command Rota Spain and the FDA: common questions

Has U.S. Navy Medicine Readiness And Training Command Rota Spain received an FDA warning letter?

No FDA warning letter addressed to the name "U.S. Navy Medicine Readiness And Training Command Rota Spain" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has U.S. Navy Medicine Readiness And Training Command Rota Spain received an FDA Form 483?

FDA has not published a Form 483 for "U.S. Navy Medicine Readiness And Training Command Rota Spain" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect U.S. Navy Medicine Readiness And Training Command Rota Spain?

The most recent FDA inspection on file ended Aug 7, 2025 at Rota, Spain and was classified NAI. FDA has 8 inspections of U.S. Navy Medicine Readiness And Training Command Rota Spain on file.

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