Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
FDA inspection history in Ravensburg, Germany, 2017 to 2024
- 5
- Form 483s
Every document, by year
- Form 483
2017: one Form 483; 2018: one Form 483; 2019: one Form 483; 2022: one Form 483; 2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017–19Three Form 483s, at Ravensburg, Germany.
- 2017The longest 483 on file: 4 observations over 4 pages at Ravensburg, Germany.
- 2022–24Two Form 483s, at Ravensburg, Germany.
Cited most
Across all Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.122Materials examination and usage criteria1
- 21 CFR 211.186Master production and control records1
The complete Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) file.
All 5 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
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Sites
Ravensburg, Germany
Five Form 483s · 2017 to 2024 · 13 observations
Latest: Form 483, Mar 19, 2024 →
Documents
5 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-03-19 | 483 Form 483 | Ravensburg, Germany | 4 | $99 |
| 2022-08-26 | 483 Form 483 | Ravensburg, Germany | 3 | $99 |
| 2019-07-17 | 483 Form 483 | Ravensburg, Germany | 1 | $99 |
| 2018-02-09 | 483 Form 483 | Ravensburg, Germany | 1 | $99 |
| 2017-11-02 | 483 Form 483 | Ravensburg, Germany | 4 | $99 |
Investigators on these documents
Ashley Queen (1)Bo Chi (1)Leiyun Boone (1)Michael R. Klapal (1)Michael R. Shanks (1)Mihaly S. Ligmond (1)Olumide Martins (1)Simone E. Pitts (1)Thuy T. Nguyen (1)Wayne Seifert (1)Zonglin Hu (1)
FEI number 3005987757 · most recent document Mar 19, 2024
About Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)
How many FDA Form 483s has Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) received?
FDA Intel has 5 Form 483s on file for Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen); the most recent is dated Mar 19, 2024.
When was Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) last inspected by FDA?
The most recent FDA inspection document on file for Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) is a Form 483 dated Mar 19, 2024, for the site in Ravensburg, Germany.
What did FDA cite at Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen)?
The regulations cited most in the observations on file for Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen) are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time.