Perrigo Holland Inc.
FDA inspection history in Holland, Michigan, 2009 to 2019
- 2
- EIRs
- 1
- Form 483
Every document, by year
- Form 483
- EIR
2009: one inspection report; 2010: one inspection report; 2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2009–10Two inspection reports, at Holland, Michigan.
- 2019One Form 483, at Holland, Michigan.
Cited most
Across all Perrigo Holland observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.188Batch production and control records1
- 21 CFR 211.192Production record review1
- 21 CFR 211.194Laboratory records1
- 21 CFR 211.42Design and construction features1
The complete Perrigo Holland file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Holland, Michigan
Two inspection reports and one Form 483 · 2009 to 2019 · 6 observations
Latest: Form 483, Oct 22, 2019 →
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-10-22 | 483 Form 483 | Holland, Michigan | 6 | $99 |
| 2010-04-20 | EIR EIR | Holland, Michigan | — | $550 |
| 2009-06-03 | EIR EIR | Holland, Michigan | — | $550 |
Investigators on these documents
Martha Sullivan Myrick (2)Charles L. Zhou (1)Lindsey M. Schwierjohann (1)
FEI number 1000518646 · most recent document Oct 22, 2019
About Perrigo Holland Inc.
How many FDA Form 483s has Perrigo Holland Inc. received?
FDA Intel has 1 Form 483 on file for Perrigo Holland Inc.; the most recent is dated Oct 22, 2019.
When was Perrigo Holland Inc. last inspected by FDA?
The most recent FDA inspection document on file for Perrigo Holland Inc. is a Form 483 dated Oct 22, 2019, for the site in Holland, Michigan.
What did FDA cite at Perrigo Holland Inc.?
The regulations cited most in the observations on file for Perrigo Holland Inc. are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.188 (Batch production and control records), 1 time; 21 CFR 211.192 (Production record review), 1 time.