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R-Pharm Germany GmbH FDA Record

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

R-Pharm Germany GmbH has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "R-Pharm Germany GmbH" is on file.

What these totals cover: FDA records filed under the name "R-Pharm Germany GmbH" and its spelling variant "R-Pharm Germany".

Latest inspection: Feb 28, 2023 · VAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	4	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

R-Pharm Germany GmbH's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	0	0	0	0	0
2024	0	0	0	0	0
2023	1	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	1	0	0	0	0
2018	0	0	0	0	0
2017	0	0	0	0	0

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

4 inspections from Jun 18, 2010 to Feb 28, 2023.

Date	Site	Product	Classification	FEI
Feb 28, 2023	Illertissen, Germany	Drugs	Voluntary Action Indicated (VAI)	3002807165
Aug 1, 2019	Illertissen, Germany	Drugs	No Action Indicated (NAI)	3002807165
Nov 7, 2014	Illertissen, Germany	Drugs	Voluntary Action Indicated (VAI)	3002807165
Jun 18, 2010	Illertissen, Germany	Drugs	No Action Indicated (NAI)	3002807165

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.

Facility	Location	Inspections	Latest
FEI 3002807165	Illertissen, Germany	4	Feb 28, 2023

R-Pharm Germany GmbH and the FDA: common questions

Has R-Pharm Germany GmbH received an FDA warning letter?

No FDA warning letter addressed to the name "R-Pharm Germany GmbH" 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 R-Pharm Germany GmbH received an FDA Form 483?

FDA has not published a Form 483 for "R-Pharm Germany GmbH" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect R-Pharm Germany GmbH?

The most recent FDA inspection on file ended Feb 28, 2023 at Illertissen, Germany and was classified VAI. FDA has 4 inspections of R-Pharm Germany GmbH on file.

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