Allermed Laboratories, Inc.
FDA inspection history in San Diego, California, 2017
- 1
- Form 483
Every document, by year
- Form 483
2017: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2017One Form 483, at San Diego, California.
Cited most
Across all Allermed Laboratories observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.100Written procedures; deviations1
The complete Allermed Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
San Diego, California
One Form 483 · 2017 · 3 observations
Latest: Form 483, Jun 14, 2017 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2017-06-14 | 483 Form 483 | San Diego, California | 3 | $99 |
Investigators on these documents
FEI number 1000098920 · most recent document Jun 14, 2017
About Allermed Laboratories, Inc.
How many FDA Form 483s has Allermed Laboratories, Inc. received?
FDA Intel has 1 Form 483 on file for Allermed Laboratories, Inc.; the most recent is dated Jun 14, 2017.
When was Allermed Laboratories, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Allermed Laboratories, Inc. is a Form 483 dated Jun 14, 2017, for the site in San Diego, California.
What did FDA cite at Allermed Laboratories, Inc.?
The regulations cited most in the observations on file for Allermed Laboratories, Inc. are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.100 (Written procedures; deviations), 1 time.