Aspen Oss B.V.
FDA inspection history in Boxtel, Netherlands, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Boxtel, Netherlands.
Cited most
Across all Aspen Oss B.V. observations on file
- 21 CFR 211.110Sampling and testing of in-process materials and drug products1
- 21 CFR 211.170Reserve samples1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
The complete Aspen Oss B.V. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Boxtel, Netherlands
One Form 483 · 2019 · 4 observations
Latest: Form 483, Sep 13, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-09-13 | 483 Form 483 | Boxtel, Netherlands | 4 | $99 |
Investigators on these documents
FEI number 3010414279 · most recent document Sep 13, 2019
About Aspen Oss B.V.
How many FDA Form 483s has Aspen Oss B.V. received?
FDA Intel has 1 Form 483 on file for Aspen Oss B.V.; the most recent is dated Sep 13, 2019.
When was Aspen Oss B.V. last inspected by FDA?
The most recent FDA inspection document on file for Aspen Oss B.V. is a Form 483 dated Sep 13, 2019, for the site in Boxtel, Netherlands.
What did FDA cite at Aspen Oss B.V.?
The regulations cited most in the observations on file for Aspen Oss B.V. are 21 CFR 211.110 (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.170 (Reserve samples), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time.